Captopril - 53808-0348-1 - (Captopril)

Alphabetical Index


Drug Information of Captopril

Product NDC: 53808-0348
Proprietary Name: Captopril
Non Proprietary Name: Captopril
Active Ingredient(s): 100    mg/1 & nbsp;   Captopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Captopril

Product NDC: 53808-0348
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074505
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Captopril

Package NDC: 53808-0348-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0348-1)

NDC Information of Captopril

NDC Code 53808-0348-1
Proprietary Name Captopril
Package Description 30 TABLET in 1 BLISTER PACK (53808-0348-1)
Product NDC 53808-0348
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Captopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name CAPTOPRIL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Captopril


General Information