Hikal
NDC Database
Hikal
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 34
- Latest Marketing Date 2026-05-20
- Data Source FDA
- First Marketing Date 2015-01-12
Company Overview
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Company Snapshot
Hikal
Great Eastern ChambersSector 11, CBD-BelapurNavi MumbaiIndia - 400 614
India
www.hikal.com/ enquiries@pharmacompass.com View on MapNDC Records ( 34 records )
Nonproprietary Name
Vildagliptin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
VILDAGLIPTIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CELECOXIB
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
CELECOXIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-09-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rivaroxaban
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
RIVAROXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-08-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
GABAPENTIN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
GABAPENTIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BUPROPION HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
BUPROPION HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ONDANSETRON HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
ONDANSETRON HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ONDANSETRON
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
ONDANSETRON
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
GEMFIBROZIL
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
GEMFIBROZIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TRIPROLIDINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
TRIPROLIDINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DECOQUINATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
DECOQUINATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
VENLAFAXINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
VENLAFAXINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
MEMANTINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
MEMANTINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
QUETIAPINE FUMARATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
QUETIAPINE FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PENTOXIFYLLINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
PENTOXIFYLLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-08-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LACOSAMIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
LACOSAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
CV
Start Marketing Date
2017-07-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PREGABALIN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
PREGABALIN
Product Type
BULK INGREDIENT
DEA Schedule
CV
Start Marketing Date
2017-07-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
VALACYCLOVIR HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
VALACYCLOVIR HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-07-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SITAGLIPTIN PHOSPHATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
SITAGLIPTIN PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-07-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DABIGATRAN ETEXILATE MESYLATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
DABIGATRAN ETEXILATE MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-07-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CELECOXIB
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
CELECOXIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-07-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BUTORPHANOL TARTRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
BUTORPHANOL TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
CIV
Start Marketing Date
2017-07-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
APIXABAN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
APIXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PYRIMETHAMINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
PYRIMETHAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SITAGLIPTIN HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
SITAGLIPTIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-09-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DAPAGLIFLOZIN PROPANEDIOL
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
DAPAGLIFLOZIN PROPANEDIOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SITAGLIPTIN PHOSPHATE ANHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
SITAGLIPTIN PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-10-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ERTUGLIFLOZIN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
ERTUGLIFLOZIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Desvenlafaxine Succinate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
DESVENLAFAXINE SUCCINATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-08-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bupropion Hydrobromide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
BUPROPION HYDROBROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-04-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bupropion Hydrobromide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
BUPROPION HYDROBROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-06-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Edoxaban Tosylate Monohydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
EDOXABAN TOSYLATE MONOHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-10-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lubabegron fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
LUBABEGRON FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-03-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vonoprazan Fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
VONOPRAZAN FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-05-20
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Cariprazine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HIKAL LIMITED
Marketing Category
BULK INGREDIENT
Substance
CARIPRAZINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-05-20
End Marketing Date
-
Listing Record Certified Through
2027-12-31
NDC Type Breakdown
34 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
66651-102
Nonproprietary Name
Vildagliptin
Labeler
HIKAL LIMITED
Dosage Form
POWDER
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