Ramipril
These highlights do not include all the information needed to use Ramipril Capsules USP safely and effectively. See full prescribing information for Ramipril Capsules USP. Ramipril Capsules USP, Oral Initial U.S. Approval: 1991
Approved
Approval ID
1dc2b41e-97c5-415b-e054-00144ff8d46c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 27, 2019
Manufacturers
FDA
Medsource Pharmaceuticals
DUNS: 833685915
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ramipril
PRODUCT DETAILS
NDC Product Code45865-441
Application NumberANDA077900
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateDecember 27, 2019
Generic NameRamipril
INGREDIENTS (6)
D&C RED NO. 28Inactive
Code: 767IP0Y5NH
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
GELATINInactive
Code: 2G86QN327L
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
RAMIPRILActive
Quantity: 10 mg in 1 1
Code: L35JN3I7SJ
Classification: ACTIB