USV Private Limited
NDC Database
USV Private Limited
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 43
- Latest Marketing Date 2024-12-12
- Data Source FDA
- First Marketing Date 2009-08-05
Company Overview
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Company Snapshot
USV Private Limited
Arvind Vithal Gandhi Chowk, BSD Marg, Station Road, Govandi East, Mumbai
India
www.usvpeptides.com/ custompeptides@usv.in View on MapNDC Records ( 43 records )
Nonproprietary Name
Glipizide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
GLIPIZIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-09-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Glyburide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
GLYBURIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-09-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pioglitazone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
PIOGLITAZONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-02-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ropinirole Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
ROPINIROLE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-02-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Glimepiride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
GLIMEPIRIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-09-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Donepezil Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
DONEPEZIL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Repaglinide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
REPAGLINIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ropinirole Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
ROPINIROLE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-01-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Metformin Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
METFORMIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-04-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pioglitazone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
PIOGLITAZONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-02-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Donepezil Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
DONEPEZIL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Repaglinide
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
REPAGLINIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Atovaquone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
ATOVAQUONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pioglitazone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
PIOGLITAZONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pioglitazone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
PIOGLITAZONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Imiquimod
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
IMIQUIMOD
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nateglinide Micronised
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
NATEGLINIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Imiquimod
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
IMIQUIMOD
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-11-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dolasetron Mesylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
DOLASETRON MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dolasetron Mesylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
DOLASETRON MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Metformin Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
METFORMIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-03-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Metformin Hydrochloride
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
METFORMIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-04-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Metformin Hydrochloride
Dosage Form
GRANULE
Strength
100 kg/100kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
METFORMIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-04-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Olopatadine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
OLOPATADINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Olopatadine Hydrochloride
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
OLOPATADINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zoledronic Acid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
ZOLEDRONIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-01-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acitretin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
ACITRETIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-11-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acitretin
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
ACITRETIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Naratriptan Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
NARATRIPTAN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Metformin Hydrochloride
Dosage Form
GRANULE
Strength
25 kg/25kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
METFORMIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-07-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Octreotide
Dosage Form
POWDER
Strength
100 g/100g
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
OCTREOTIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Palonosetron Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
PALONOSETRON HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-04-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Icatibant Acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
ICATIBANT ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sugammadex Sodium
Dosage Form
POWDER
Strength
50 kg/50kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
SUGAMMADEX SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Trimetazidine Dihydrochloride
Dosage Form
POWDER
Strength
50 kg/50kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
TRIMETAZIDINE DIHYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-12-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ticagrelor
Dosage Form
POWDER
Strength
50 kg/50kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
TICAGRELOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-12-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Etelcalcetide Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
ETELCALCETIDE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-12-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dapagliflozin (Dapagliflozin 30% w/w solution in Isopropyl alcohol)
Dosage Form
LIQUID
Strength
10 g/10g
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
DAPAGLIFLOZIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-11-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rivaroxan
Dosage Form
POWDER
Strength
50 kg/50kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
RIVAROXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-12-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Empagliflozin
Dosage Form
POWDER
Strength
50 kg/50kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
EMPAGLIFLOZIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-12-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Regadenoson
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
REGADENOSON
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-12-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Glimepiride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
GLIMEPIRIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-09-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
glipizide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
USV Private Limited
Marketing Category
BULK INGREDIENT
Substance
GLIPIZIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-08-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
43 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
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NDC
62147-0001
Nonproprietary Name
Glipizide
Labeler
USV Private Limited
Dosage Form
POWDER
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