PREDNISONE

Product NDC: 71329-105
11-digit product format: 713290105
Labeler code: 71329
Product ID: 71329-105_c3dd4f62-cc06-4576-938c-c50f5a4a1642
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Prednisone
Dosage form: TABLET
Route: ORAL
Labeler: GeneYork Pharmaceuticals Group LLC
Application: ANDA210525
Marketing category: ANDA
Marketing start: 2018-12-04
Marketing end: 0000-00-00
Substance: PREDNISONE
Active strength: 50 mg/1
Pharmacologic classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71329-105-01	2022-10-19	C162847	48780-1	e4f33bdf-9b66-d8a0-e053-dadaa90a6e4e	bbc5e24a-ba0f-4f7e-be39-a1995fd96d5b
71329-105-01	2022-07-29	C162847	48780-1	e4f33bdf-9b66-d8a0-e053-dadaa90a6e4e	bbc5e24a-ba0f-4f7e-be39-a1995fd96d5b

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
VB0R961HZT	PREDNISONE	53-03-2	PREDNISONE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
71329-105-01	71329010501	1 BOTTLE, PLASTIC in 1 CARTON (71329-105-01) > 100 TABLET in 1 BOTTLE, PLASTIC	2018-12-04	0000-00-00	No	No	Current