Zidovudine

Product NDC: 52343-044
11-digit product format: 523430044
Labeler code: 52343
Product ID: 52343-044_f238bbef-cbea-49ed-8e09-8c0fa73b4f36
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Zidovudine
Dosage form: CAPSULE
Route: ORAL
Labeler: ACETRIS HEALTH, LLC
Application: ANDA078128
Marketing category: ANDA
Marketing start: 2006-03-27
Marketing end: 0000-00-00
Substance: ZIDOVUDINE
Active strength: 100 mg/1
Pharmacologic classes: Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
52343-044-01	EA - Each	52343-044	eaec7c24-dc81-42c8-9b1a-269f0b890d18	1	2013-09-04

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4B9XT59T7S	ZIDOVUDINE	30516-87-1	ZIDOVUDINE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52343-044-01	52343004401	100 CAPSULE in 1 BOTTLE (52343-044-01)	100 capsule	2006-03-27	0000-00-00	No	No	Current