PRAVASTATIN SODIUM

Product NDC
60429-368
11-digit product format
604290368
Labeler code
60429
Product ID
60429-368_a58d190c-dd8b-3b3f-e053-2a95a90a148b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PRAVASTATIN SODIUM
Dosage form
TABLET
Route
ORAL
Labeler
Golden State Medical Supply
Application
ANDA076341
Marketing category
ANDA
Marketing start
2006-10-23
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
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60429-368-05EA - Each60429-368192fe0c2-53fa-4041-b2a1-8e60a6ff969612012-07-24
60429-368-45EA - Each60429-368908162c6-41b1-4351-8fd0-b923b7671c6e12013-11-04
60429-368-90EA - Each60429-368c5c84ee2-2144-4c29-b302-3c7553a3688c12012-07-24