PRAVASTATIN SODIUM

Product NDC: 63629-7086
11-digit product format: 636297086
Labeler code: 63629
Product ID: 63629-7086_2abc4689-42f7-4641-9196-7e1dbdd9f64c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: PRAVASTATIN SODIUM
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA077491
Marketing category: ANDA
Marketing start: 2014-07-28
Marketing end: 0000-00-00
Substance: PRAVASTATIN SODIUM
Active strength: 80 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
63629-7086-1	2020-10-16	C162847	48780-1	9d75b9d0-2971-f424-e053-dadaa90a57ce	e5b461f8-e044-47b3-b3bd-1c0a24de454d
63629-7086-1	2020-01-31	C162847	48780-1	9d75b9d0-2971-f424-e053-dadaa90a57ce	e5b461f8-e044-47b3-b3bd-1c0a24de454d

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
63629-7086-1	63629708601	30 TABLET in 1 BOTTLE (63629-7086-1)	30 tablet	2016-09-16	0000-00-00	No	No	Current