PRAVASTATIN SODIUM

Product NDC
0781-5232
11-digit product format
007815232
Labeler code
0781
Product ID
0781-5232_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
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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-5232-10EA - Each0781-52323504c0bf-d0c5-430a-a236-6580e9f7cac412022-06-06
0781-5232-92EA - Each0781-5232ea4afbda-81f7-45b8-80ee-71ec89db24cd12014-04-03