Pravastatin Sodium

Product NDC
0615-6557
11-digit product format
006156557
Labeler code
0615
Product ID
0615-6557_18862fca-d643-474b-b1af-6af180f2c45f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pravastain Sodium
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA076056
Marketing category
ANDA
Marketing start
2011-07-22
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
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-6557-392021-08-10C16284748780-197449f38-cfb6-f6ea-e053-dbdaa90aa703b4a580e1-5eef-4400-b4de-0a478d668df3
0615-6557-392019-11-13C16284748780-197449f38-cfb6-f6ea-e053-dbdaa90aa703b4a580e1-5eef-4400-b4de-0a478d668df3