PRAVASTATIN SODIUM

Product NDC
0781-5234
11-digit product format
007815234
Labeler code
0781
Product ID
0781-5234_56c39347-1ea1-4306-bd14-dda785df7143
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PRAVASTATIN SODIUM
Dosage form
TABLET
Route
ORAL
Labeler
Sandoz Inc
Application
ANDA076397
Marketing category
ANDA
Marketing start
2014-04-28
Marketing end
0000-00-00
Substance
PRAVASTATIN SODIUM
Active strength
40 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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-5234-10EA - Each0781-523436fde735-a1ab-4aa1-94be-d60166bf208c12022-06-06
0781-5234-92EA - Each0781-52340eafc057-0d52-45eb-930f-1ef5c201040112014-05-02