Biocon
NDC Database

Biocon

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 62
  • Latest Marketing Date 2026-03-20
  • Data Source FDA
  • First Marketing Date 2000-01-01
Company Overview

Company

Biocon

Country

India

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Biocon

Hosur Road,Electronics City,Bangalore

India

www.biocon.com/ contact.us@biocon.com View on Map
NDC Records ( 62 records )
2000
01 Jan
Bulk Ingredient NDC: 65727-002

Nonproprietary Name

Simvastatin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-002

Substance

SIMVASTATIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
01 Jan
Bulk Ingredient NDC: 65727-003

Nonproprietary Name

Pravastatin Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-003

Substance

PRAVASTATIN SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
01 Jan
Bulk Ingredient NDC: 65727-004

Nonproprietary Name

Atorvastatin calcium crystalline

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-004

Substance

ATORVASTATIN CALCIUM TRIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
01 Jan
Bulk Ingredient NDC: 65727-005

Nonproprietary Name

Mycophenolate Mofetil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-005

Substance

MYCOPHENOLATE MOFETIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
01 Jan
Bulk Ingredient NDC: 65727-009

Nonproprietary Name

Tacrolimus

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-009

Substance

TACROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
01 Jan
Bulk Ingredient NDC: 65727-010

Nonproprietary Name

Repaglinide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-010

Substance

REPAGLINIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
01 Jan
Bulk Ingredient NDC: 65727-011

Nonproprietary Name

Mycophenolic Acid

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-011

Substance

MYCOPHENOLIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
01 Jan
Bulk Ingredient NDC: 65727-012

Nonproprietary Name

Fluvastatin Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-012

Substance

FLUVASTATIN SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
01 Jan
Bulk Ingredient NDC: 65727-013

Nonproprietary Name

Sirolimus

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-013

Substance

SIROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
15 Sep
Bulk Ingredient NDC: 65727-015

Nonproprietary Name

ORLISTST

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

BIOCON LIMITED

Marketing Category

BULK INGREDIENT

65727-015

Substance

ORLISTAT

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-09-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
01 Jan
Bulk Ingredient NDC: 65727-017

Nonproprietary Name

Fluvastatin sodium Amorphous

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-017

Substance

FLUVASTATIN SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
01 Jan
Bulk Ingredient NDC: 65727-019

Nonproprietary Name

Mycophenolate Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-019

Substance

MYCOPHENOLATE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2005
01 Jan
Bulk Ingredient NDC: 65727-023

Nonproprietary Name

Insulin Glargine (rDNA Origin) - Bulk

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-023

Substance

INSULIN GLARGINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-01-01

End Marketing Date

2026-06-30

Listing Record Certified Through

-

2009
01 Jan
Bulk Ingredient NDC: 65727-027

Nonproprietary Name

Fidaxomicin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-027

Substance

FIDAXOMICIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
13 Jan
Bulk Ingredient NDC: 65727-028

Nonproprietary Name

Rosuvastatin Calcium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-028

Substance

ROSUVASTATIN CALCIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-01-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
30 Nov
Bulk Ingredient NDC: 65727-033

Nonproprietary Name

Brinzolamide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-033

Substance

BRINZOLAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-11-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
01 Nov
Bulk Ingredient NDC: 65727-036

Nonproprietary Name

Fingolimod hydrochloride

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

BIOCON LIMITED

Marketing Category

BULK INGREDIENT

65727-036

Substance

FINGOLIMOD HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
12 Feb
Bulk Ingredient NDC: 65727-037

Nonproprietary Name

Deferasirox

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-037

Substance

DEFERASIROX

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-02-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
05 Jul
Bulk Ingredient NDC: 65727-038

Nonproprietary Name

Glatiramer acetate

Dosage Form

POWDER

Strength

2 kg/2kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-038

Substance

GLATIRAMER ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-07-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Sep
Bulk Ingredient NDC: 65727-045

Nonproprietary Name

Pimecrolimus

Dosage Form

POWDER

Strength

10 kg/10kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-045

Substance

PIMECROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
15 Sep
Bulk Ingredient NDC: 65727-046

Nonproprietary Name

Everolimus

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-046

Substance

EVEROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-09-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
15 Jan
Bulk Ingredient NDC: 65727-048

Nonproprietary Name

Mirabegron

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon limited

Marketing Category

BULK INGREDIENT

65727-048

Substance

MIRABEGRON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-01-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
15 Apr
Bulk Ingredient NDC: 65727-049

Nonproprietary Name

Dabigatran

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-049

Substance

DABIGATRAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-04-15

End Marketing Date

2027-03-15

Listing Record Certified Through

-

2021
29 Aug
Bulk Ingredient NDC: 65727-050

Nonproprietary Name

Rivaroxaban

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-050

Substance

RIVAROXABAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-08-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
01 Oct
Bulk Ingredient NDC: 65727-051

Nonproprietary Name

Vildagliptin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-051

Substance

VILDAGLIPTIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Mar
Bulk Ingredient NDC: 65727-053

Nonproprietary Name

Sitagliptin phosphate monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-053

Substance

SITAGLIPTIN PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
15 Mar
Bulk Ingredient NDC: 65727-055

Nonproprietary Name

Micafungin sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon limited

Marketing Category

BULK INGREDIENT

65727-055

Substance

MICAFUNGIN SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-03-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
05 Sep
Bulk Ingredient NDC: 65727-057

Nonproprietary Name

Linagliptin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-057

Substance

LINAGLIPTIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-09-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
16 Nov
Bulk Ingredient NDC: 65727-058

Nonproprietary Name

Teriflunomide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-058

Substance

TERIFLUNOMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
14 Mar
Bulk Ingredient NDC: 65727-059

Nonproprietary Name

Posaconazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-059

Substance

POSACONAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-03-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
01 Sep
Bulk Ingredient NDC: 65727-063

Nonproprietary Name

Everolimus

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-063

Substance

EVEROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
01 Oct
Bulk Ingredient NDC: 65727-064

Nonproprietary Name

Everolimus

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon limited

Marketing Category

BULK INGREDIENT

65727-064

Substance

EVEROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Dec
Bulk Ingredient NDC: 65727-071

Nonproprietary Name

Sitagliptin hydrochloride

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

BIOCON LIMITED

Marketing Category

BULK INGREDIENT

65727-071

Substance

SITAGLIPTIN HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
11 Aug
Bulk Ingredient NDC: 65727-072

Nonproprietary Name

Anidulafungin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-072

Substance

ANIDULAFUNGIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-08-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
02 Jul
Bulk Ingredient NDC: 65727-073

Nonproprietary Name

Dapagliflozin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-073

Substance

DAPAGLIFLOZIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-07-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
03 May
Bulk Ingredient NDC: 65727-078

Nonproprietary Name

Sitagliptin phosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-078

Substance

SITAGLIPTIN PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-05-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
15 Apr
Bulk Ingredient NDC: 65727-079

Nonproprietary Name

Sacubitril

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-079

Substance

SACUBITRIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-04-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
02 May
Bulk Ingredient NDC: 65727-080

Nonproprietary Name

Valsartan

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-080

Substance

VALSARTAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-05-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
27 Aug
Bulk Ingredient NDC: 65727-081

Nonproprietary Name

Apixaban

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-081

Substance

APIXABAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-08-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
09 Feb
Bulk Ingredient NDC: 65727-084

Nonproprietary Name

Lenalidomide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-084

Substance

LENALIDOMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Dec
Bulk Ingredient NDC: 65727-085

Nonproprietary Name

Empagliflozin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-085

Substance

EMPAGLIFLOZIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
07 Nov
Bulk Ingredient NDC: 65727-086

Nonproprietary Name

Everolimus Premix 2 %

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-086

Substance

EVEROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-11-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
26 Aug
Bulk Ingredient NDC: 65727-087

Nonproprietary Name

Liraglutide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-087

Substance

LIRAGLUTIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-08-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
17 Nov
Bulk Ingredient NDC: 65727-088

Nonproprietary Name

Dasatinib monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-088

Substance

DASATINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
24 Jul
Bulk Ingredient NDC: 65727-091

Nonproprietary Name

Cabozantinib-(S)-Malate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-091

Substance

CABOZANTINIB S-MALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-07-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
01 Mar
Bulk Ingredient NDC: 65727-092

Nonproprietary Name

Dapagliflozin Propane Diol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-092

Substance

DAPAGLIFLOZIN PROPANEDIOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
01 Mar
Bulk Ingredient NDC: 65727-093

Nonproprietary Name

Orlistat pellets

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Biocon limited

Marketing Category

BULK INGREDIENT

65727-093

Substance

ORLISTAT

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
17 Sep
Bulk Ingredient NDC: 65727-094

Nonproprietary Name

Semaglutide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-094

Substance

SEMAGLUTIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-09-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
22 Feb
Bulk Ingredient NDC: 65727-095

Nonproprietary Name

Ivacaftor

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-095

Substance

IVACAFTOR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-02-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
18 Mar
Bulk Ingredient NDC: 65727-096

Nonproprietary Name

LURASIDONE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-096

Substance

LURASIDONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-03-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
07 Dec
Bulk Ingredient NDC: 65727-097

Nonproprietary Name

Lenalidomide hemihydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-097

Substance

LENALIDOMIDE HEMIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-12-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
29 Nov
Bulk Ingredient NDC: 65727-098

Nonproprietary Name

Eltrombopag Olamine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-098

Substance

ELTROMBOPAG OLAMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-11-29

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
12 Mar
Bulk Ingredient NDC: 65727-101

Nonproprietary Name

Tacrolimus

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-101

Substance

TACROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-03-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
25 Mar
Bulk Ingredient NDC: 65727-103

Nonproprietary Name

OLAPARIB

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-103

Substance

OLAPARIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-03-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
26 Mar
Bulk Ingredient NDC: 65727-104

Nonproprietary Name

Nintedanib Esylate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-104

Substance

NINTEDANIB ESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-03-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2018
25 Aug
Bulk Ingredient NDC: 65727-105

Nonproprietary Name

DABIGATRAN ETEXILATE MESYLATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-105

Substance

DABIGATRAN ETEXILATE MESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-08-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
26 Aug
Bulk Ingredient NDC: 65727-106

Nonproprietary Name

Tacrolimus Granules 20% w/w

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-106

Substance

TACROLIMUS ANHYDROUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-08-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Apr
Bulk Ingredient NDC: 65727-107

Nonproprietary Name

Posaconazole (Form- 1)

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-107

Substance

POSACONAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
22 Oct
Bulk Ingredient NDC: 65727-109

Nonproprietary Name

TIRZEPATIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

BIOCON LIMITED

Marketing Category

BULK INGREDIENT

65727-109

Substance

TIRZEPATIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-10-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
28 Aug
Bulk Ingredient NDC: 65727-110

Nonproprietary Name

Enzalutamide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-110

Substance

ENZALUTAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-08-28

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
27 Feb
Bulk Ingredient NDC: 65727-113

Nonproprietary Name

Edoxaban Tosylate Monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-113

Substance

EDOXABAN TOSYLATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-02-27

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
20 Mar
Bulk Ingredient NDC: 65727-115

Nonproprietary Name

Trametinib Dimethylsulfoxide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biocon Limited

Marketing Category

BULK INGREDIENT

65727-115

Substance

TRAMETINIB DIMETHYL SULFOXIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-03-20

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
62 total
  • Bulk Ingredient
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

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NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

65727-002

Nonproprietary Name

Simvastatin

Labeler

Biocon Limited

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

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Data maintained from official sources

Structured Database

Searchable pharmaceutical data

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NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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