Captopril

Product NDC

70518-0406

11-digit product format

705180406

Labeler code

70518

Product ID

70518-0406_848cf5d3-3ceb-a19c-e053-2991aa0af469

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

captopril

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA074434

Marketing category

ANDA

Marketing start

2017-04-05

Marketing end

0000-00-00

Substance

CAPTOPRIL

Active strength

25 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record