PRAVASTATIN SODIUM

Product NDC

50436-3800

11-digit product format

504363800

Labeler code

50436

Product ID

50436-3800_e6bd46d6-fe7d-44c2-81d0-4744cc6a0f0e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PRAVASTATIN SODIUM

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA076341

Marketing category

ANDA

Marketing start

2011-07-18

Marketing end

0000-00-00

Substance

PRAVASTATIN SODIUM

Active strength

20 mg/1

Pharmacologic classes

HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record