VIDEX

Product NDC: 0087-6632
11-digit product format: 000876632
Labeler code: 0087
Product ID: 0087-6632_107740fb-6b19-4480-bf38-a8848d8abee9
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: didanosine
Dosage form: POWDER, FOR SOLUTION
Route: ORAL
Labeler: Bristol-Myers Squibb Company
Application: NDA020156
Marketing category: NDA
Marketing start: 1991-10-09
Marketing end: 2021-02-28
Substance: DIDANOSINE
Active strength: 10 mg/mL
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: 0000-00-00
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
0087-6632-41	ML - Milliliter	0087-6632	87d86f0f-0e94-4779-80ad-eefc343694fc	1	2012-07-24

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
K3GDH6OH08	DIDANOSINE	69655-05-6	DIDANOSINE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0087-6632-41	00087663241	1 BOTTLE in 1 CARTON (0087-6632-41) > 200 mL in 1 BOTTLE	1 bottle	1991-10-09	2021-02-28	No	No	Current