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Last Updated: November 13, 2024

Details for New Drug Application (NDA): 074737


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NDA 074737 describes CAPTOPRIL, which is a drug marketed by Ajanta Pharma Ltd, Andas 5 Holding, Apothecon, Aurobindo Pharma Usa, Changzhou Pharm, Chartwell Rx, Corepharma, Cosette, Dava Pharms Inc, Egis Pharms, G And W Labs Inc, Hikma Intl Pharms, Oxford Pharms, Prinston Inc, Purepac Pharm, Sandoz, Seton Pharms, Strides Pharma, Teva, Watson Labs, Wockhardt, Ivax Sub Teva Pharms, and Rising, and is included in thirty-one NDAs. It is available from thirteen suppliers. Additional details are available on the CAPTOPRIL profile page.

The generic ingredient in CAPTOPRIL is captopril; hydrochlorothiazide. There are fifteen drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the captopril; hydrochlorothiazide profile page.
Summary for 074737
Tradename:CAPTOPRIL
Applicant:Corepharma
Ingredient:captopril
Patents:0
Pharmacology for NDA: 074737
Medical Subject Heading (MeSH) Categories for 074737
Suppliers and Packaging for NDA: 074737
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
CAPTOPRIL captopril TABLET;ORAL 074737 ANDA Camber Pharmaceuticals, Inc. 31722-141 31722-141-01 100 TABLET in 1 BOTTLE (31722-141-01)
CAPTOPRIL captopril TABLET;ORAL 074737 ANDA Camber Pharmaceuticals, Inc. 31722-141 31722-141-10 1000 TABLET in 1 BOTTLE (31722-141-10)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength12.5MG
Approval Date:Oct 28, 1998TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength25MG
Approval Date:Oct 28, 1998TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength50MG
Approval Date:Oct 28, 1998TE:ABRLD:No

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