Alembic Pharmaceuticals Limited
NDC Database
Alembic Pharmaceuticals Limited
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 20
- Latest Marketing Date 2026-01-12
- Data Source FDA
- First Marketing Date 2010-06-08
Company Overview
Company
Alembic Pharmaceuticals Limited
Country
India
Website
Social Profiles
Company Snapshot
Alembic Pharmaceuticals Limited
Alembic Road, Vadodara - 390 003, Gujarat
India
www.alembic-india.com/ infoal@alembic.co.in View on MapNDC Records ( 20 records )
Nonproprietary Name
ERYTHROMYCIN
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
ERYTHROMYCIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-10-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Clonidine
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
CLONIDINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-10-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ARIPIPRAZOLE
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
ARIPIPRAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-01-12
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
CLARITHROMYCIN
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
CLARITHROMYCIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-10-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BUPROPION HYDROCHLORIDE
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
BUPROPION HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-01-08
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Leflunomide
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
LEFLUNOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-06-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fluoxetine Hydrochloride
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
FLUOXETINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-03-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
AZITHROMYCIN MONOHYDRATE
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
AZITHROMYCIN MONOHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-01-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
FAMOTIDINE
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
FAMOTIDINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-12-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
MEXILETINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
MEXILETINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-03-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TICAGRELOR
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
TICAGRELOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-09-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CANAGLIFLOZIN
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
CANAGLIFLOZIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-10-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
RIOCIGUAT
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
RIOCIGUAT
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-04-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Afatinib Dimaleate
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
AFATINIB DIMALEATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-06-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
OLAPARIB
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
OLAPARIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-03-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Theophylline
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
THEOPHYLLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-12-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
METHOTREXATE SODIUM
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
METHOTREXATE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-01-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nelarabine
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
NELARABINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-08-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SACUBITRIL VALSARTAN TRISODIUM HEMIPENTAHYDRATE
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
SACUBITRIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-08-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ACALABRUTINIB
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Alembic Pharmaceuticals Limited
Marketing Category
BULK INGREDIENT
Substance
ACALABRUTINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-09-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
20 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 DirectoryNDC Record Details Preview
Explore important National Drug Code information available in the records above.
NDC
46708-694
Nonproprietary Name
ERYTHROMYCIN
Labeler
Alembic Pharmaceuticals Limited
Dosage Form
POWDER
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