Symed Labs
NDC Database

Symed Labs

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 37
  • Latest Marketing Date 2026-01-01
  • Data Source FDA
  • First Marketing Date 1982-01-01
Company Overview

Company

Symed Labs

Country

India

Social Profiles

LinkedIn
Company Snapshot

Symed Labs

#8-2-293/174/3, Beside BN Reddy Colony, Road No.14, Banjara Hills, Hyderabad-500034. Telangana

India

www.symedlabs.com/# marketing@symedlabs.com View on Map
NDC Records ( 37 records )
2000
18 Apr
Bulk Ingredient NDC: 66022-0103

Nonproprietary Name

Linezolid

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0103

Substance

LINEZOLID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-04-18

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1982
01 Jan
Bulk Ingredient NDC: 66022-0104

Nonproprietary Name

Hydroxyzine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0104

Substance

HYDROXYZINE DIHYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1982-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2008
27 Feb
Bulk Ingredient NDC: 66022-0105

Nonproprietary Name

Meprobamate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0105

Substance

MEPROBAMATE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2008-02-27

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2004
15 Dec
Bulk Ingredient NDC: 66022-0106

Nonproprietary Name

Eszopiclone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0106

Substance

ESZOPICLONE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2004-12-15

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2008
28 Jan
Bulk Ingredient NDC: 66022-0108

Nonproprietary Name

Levocetirizine Dihydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0108

Substance

LEVOCETIRIZINE DIHYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-01-28

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2008
28 Jan
Bulk Ingredient NDC: 66022-0108

Nonproprietary Name

Levocetirizine Dihydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0108

Substance

LEVOCETIRIZINE DIHYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-01-28

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2013
23 Aug
Bulk Ingredient NDC: 66022-0110

Nonproprietary Name

Brimonidine Tartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0110

Substance

BRIMONIDINE TARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-08-23

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1997
30 May
Bulk Ingredient NDC: 66022-0112

Nonproprietary Name

Phentermine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0112

Substance

PHENTERMINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1997-05-30

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1982
20 Jan
Bulk Ingredient NDC: 66022-0114

Nonproprietary Name

Meclizine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0114

Substance

MECLIZINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1982-01-20

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2009
06 May
Bulk Ingredient NDC: 66022-0115

Nonproprietary Name

Iloperidone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0115

Substance

ILOPERIDONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-05-06

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2004
16 Oct
Bulk Ingredient NDC: 66022-0116

Nonproprietary Name

Lanthanum Carbonate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0116

Substance

LANTHANUM CARBONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-10-16

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1992
09 Nov
Bulk Ingredient NDC: 66022-0117

Nonproprietary Name

Ketorolac Tromethamine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0117

Substance

KETOROLAC TROMETHAMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1992-11-09

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2009
01 Jul
Bulk Ingredient NDC: 66022-0118

Nonproprietary Name

Dronedarone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0118

Substance

DRONEDARONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-07-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2005
20 Mar
Bulk Ingredient NDC: 66022-0119

Nonproprietary Name

Iron Sucrose

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0119

Substance

IRON SUCROSE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-03-20

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1995
14 Sep
Bulk Ingredient NDC: 66022-0120

Nonproprietary Name

Carvedilol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0120

Substance

CARVEDILOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1995-09-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2013
28 Mar
Bulk Ingredient NDC: 66022-0121

Nonproprietary Name

Carbinoxamine Maleate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0121

Substance

CARBINOXAMINE MALEATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-03-28

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2023
23 Jun
Bulk Ingredient NDC: 66022-0122

Nonproprietary Name

Hydroxyzine Pamoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

SYMED LABS LIMITED

Marketing Category

BULK INGREDIENT

66022-0122

Substance

HYDROXYZINE PAMOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-06-23

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
01 Jan
Bulk Ingredient NDC: 66022-0123

Nonproprietary Name

Flibanserin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0123

Substance

FLIBANSERIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2000
18 Apr
Bulk Ingredient NDC: 66022-0201

Nonproprietary Name

Linezolid

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0201

Substance

LINEZOLID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-04-18

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1996
27 Nov
Bulk Ingredient NDC: 66022-0202

Nonproprietary Name

Tizanidine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0202

Substance

TIZANIDINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1996-11-27

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2011
01 Jul
Bulk Ingredient NDC: 66022-0203

Nonproprietary Name

Rivaroxaban

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0203

Substance

RIVAROXABAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-07-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1992
31 Dec
Bulk Ingredient NDC: 66022-0204

Nonproprietary Name

Ondansetron Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0204

Substance

ONDANSETRON HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1992-12-31

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1984
14 May
Bulk Ingredient NDC: 66022-0205

Nonproprietary Name

Stanozolol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0205

Substance

STANOZOLOL

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

1984-05-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1984
14 May
Bulk Ingredient NDC: 66022-0205

Nonproprietary Name

Stanozolol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0205

Substance

STANOZOLOL

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

1984-05-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1984
14 May
Bulk Ingredient NDC: 66022-0205

Nonproprietary Name

Stanozolol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0205

Substance

STANOZOLOL

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

1984-05-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2018
14 Dec
Bulk Ingredient NDC: 66022-0207

Nonproprietary Name

Prucalopride Succinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0207

Substance

PRUCALOPRIDE SUCCINATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-12-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2023
14 Oct
Bulk Ingredient NDC: 66022-0208

Nonproprietary Name

Modafinil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

SYMED LABS LIMITED

Marketing Category

BULK INGREDIENT

66022-0208

Substance

MODAFINIL

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2023-10-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2023
30 Sep
Bulk Ingredient NDC: 66022-0209

Nonproprietary Name

Hydroxychloroquine Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0209

Substance

HYDROXYCHLOROQUINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-09-30

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2023
30 Sep
Bulk Ingredient NDC: 66022-0210

Nonproprietary Name

Bilastine (Form-II)

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0210

Substance

BILASTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-09-30

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2023
30 Sep
Bulk Ingredient NDC: 66022-0211

Nonproprietary Name

Vortioxetine Hydrobromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0211

Substance

VORTIOXETINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-09-30

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2023
13 Dec
Bulk Ingredient NDC: 66022-0212

Nonproprietary Name

Ezetimibe

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0212

Substance

EZETIMIBE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-12-13

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
28 Jun
Bulk Ingredient NDC: 66022-0213

Nonproprietary Name

Bilastine (Form-I)

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0213

Substance

BILASTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-06-28

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2017
18 May
Bulk Ingredient NDC: 66022-0301

Nonproprietary Name

Deferasirox

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0301

Substance

DEFERASIROX

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-05-18

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2013
27 Nov
Bulk Ingredient NDC: 66022-0302

Nonproprietary Name

Sucroferric Oxyhydroxide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0302

Substance

FERRIC OXYHYDROXIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-11-27

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1982
01 Jan
Bulk Ingredient NDC: 66022-0303

Nonproprietary Name

Hydroxyzine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0303

Substance

HYDROXYZINE DIHYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1982-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2021
04 Oct
Bulk Ingredient NDC: 66022-0304

Nonproprietary Name

Sertraline Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0304

Substance

SERTRALINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-10-04

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
28 Jun
Bulk Ingredient NDC: 66022-0305

Nonproprietary Name

Otilonium Bromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Symed Labs Limited

Marketing Category

BULK INGREDIENT

66022-0305

Substance

OTILONIUM BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-06-28

End Marketing Date

-

Listing Record Certified Through

2027-12-31

Related Databases
  • FDA Inspections
    6 View
  • EDQM CEP
    21 View
  • KDMF
    0 View
  • Japan DMF
    2 View
  • Eudra GMP
    0 View
  • NDC Database
    37 View
  • FDA Approved Drugs Database
    0 View
  • Drug Prices in Switzerland
    0 View
NDC Type Breakdown
37 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

66022-0103

Nonproprietary Name

Linezolid

Labeler

Symed Labs 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.

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.