Captopril
Captopril Tablets, USPRev. 06/11Rx Only
Approved
Approval ID
32e7e6c1-fee7-40d4-b391-9b9f320241a8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 15, 2011
Manufacturers
FDA
RedPharm Drug Inc.
DUNS: 008039641
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Captopril
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code67296-0677
Application NumberANDA074505
Product Classification
M
Marketing Category
C73584
G
Generic Name
Captopril
Product Specifications
Route of AdministrationORAL
Effective DateAugust 15, 2011
FDA Product Classification
INGREDIENTS (7)
CAPTOPRILActive
Quantity: 15 mg in 1 1
Code: 9G64RSX1XD
Classification: ACTIB
COLLOIDAL SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
ANHYDROUS LACTOSEInactive
Code: 3SY5LH9PMK
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT