Finasteride

Product NDC: 68071-3306
11-digit product format: 680713306
Labeler code: 68071
Product ID: 68071-3306_dfaf7e4c-e69e-59c2-e053-2995a90ab7f1
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: finasteride
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: NuCare Pharmaceuticals,Inc.
Application: ANDA090121
Marketing category: ANDA
Marketing start: 2010-05-28
Marketing end: 0000-00-00
Substance: FINASTERIDE
Active strength: 5 mg/1
Pharmacologic classes: 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68071-3306-9	2021-02-12	C162847	48780-1	ba0f9c33-2dd8-a910-e053-dadaa90a0b85	5526e66a-db04-6c4d-e054-00144ff88e88
68071-3306-9	2021-01-29	C162847	48780-1	ba0f9c33-2dd8-a910-e053-dadaa90a0b85	5526e66a-db04-6c4d-e054-00144ff88e88

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
57GNO57U7G	FINASTERIDE	98319-26-7	FINASTERIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
68071-3306-9	68071330609	90 TABLET, FILM COATED in 1 BOTTLE (68071-3306-9)	2017-07-25	0000-00-00	No	No	Current