Biophore India Pharmaceuticals Pvt Ltd
NDC Database

Biophore India Pharmaceuticals Pvt Ltd

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 9
  • Latest Marketing Date 2022-12-21
  • Data Source FDA
  • First Marketing Date 2019-11-05
Company Overview

Company

Biophore India Pharmaceuticals Pvt Ltd

Country

India

Social Profiles

LinkedIn
Company Snapshot

Biophore India Pharmaceuticals Pvt Ltd

Plot#92;1-98/2/92, Kavuri Hills –Phase II, Jubilee Hills,Hyderabad 33,Telangana

India

www.biophore.com/ info@biophore.com View on Map
NDC Records ( 9 records )
2019
05 Nov
Bulk Ingredient NDC: 73435-001

Nonproprietary Name

Chlorpromazine Hydrochloride

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

Biophore India Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

73435-001

Substance

CHLORPROMAZINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
09 Dec
Bulk Ingredient NDC: 73435-002

Nonproprietary Name

Pimavanserin Tartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Biophore India Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

73435-002

Substance

PIMAVANSERIN TARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-12-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
09 Dec
Bulk Ingredient NDC: 73435-003

Nonproprietary Name

Ramelteon

Dosage Form

POWDER

Strength

10 kg/10kg

Labeler

Biophore India Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

73435-003

Substance

RAMELTEON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-12-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
09 Dec
Bulk Ingredient NDC: 73435-004

Nonproprietary Name

Obeticholic acid

Dosage Form

POWDER

Strength

10 kg/10kg

Labeler

Biophore India Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

73435-004

Substance

OBETICHOLIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-12-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
09 Dec
Bulk Ingredient NDC: 73435-005

Nonproprietary Name

Fenoprofen calcium

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Biophore India Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

73435-005

Substance

FENOPROFEN CALCIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-12-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
10 Feb
Bulk Ingredient NDC: 73435-006

Nonproprietary Name

Erythromycin Lactobionate

Dosage Form

POWDER

Strength

10 kg/10kg

Labeler

Biophore India Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

73435-006

Substance

ERYTHROMYCIN LACTOBIONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-02-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
10 Feb
Bulk Ingredient NDC: 73435-007

Nonproprietary Name

Mexiletine hydrochloride

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Biophore India Pharmaceuticals Private limited

Marketing Category

BULK INGREDIENT

73435-007

Substance

MEXILETINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-02-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
23 Dec
Bulk Ingredient NDC: 73435-012

Nonproprietary Name

Safinamide Mesylate

Dosage Form

POWDER

Strength

20 kg/20kg

Labeler

Biophore India Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

73435-012

Substance

SAFINAMIDE MESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-12-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
21 Dec
Bulk Ingredient NDC: 73435-028

Nonproprietary Name

Ethiodized Oil

Dosage Form

OIL

Strength

5 kg/5kg

Labeler

Biophore India Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

73435-028

Substance

ETHIODIZED OIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-12-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
9 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).

Visit FDA NDC Directory
NDC Record Details Preview

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

NDC

73435-001

Nonproprietary Name

Chlorpromazine Hydrochloride

Labeler

Biophore India Pharmaceuticals Private Limited

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized NDC records

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

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