Pravastatin Sodium

Product NDC: 63629-6929
11-digit product format: 636296929
Labeler code: 63629
Product ID: 63629-6929_b56e7cc4-2e04-4747-8ce1-7826f4a37e56
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Pravastatin Sodium
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA076056
Marketing category: ANDA
Marketing start: 2006-04-25
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63629-6929-1	2020-10-16	C162847	48780-1	9d75b9d0-562c-f424-e053-dadaa90a57ce	31e7ffdf-6861-4de3-b2c2-8673540568f9
63629-6929-1	2020-01-31	C162847	48780-1	9d75b9d0-562c-f424-e053-dadaa90a57ce	31e7ffdf-6861-4de3-b2c2-8673540568f9

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3M8608UQ61	PRAVASTATIN SODIUM	81131-70-6	PRAVASTATIN SODIUM

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-6929-1	63629692901	30 TABLET in 1 BOTTLE (63629-6929-1)	30 tablet	2016-02-23	0000-00-00	No	No	Current