Ondansetron

Product NDC: 63739-333
11-digit product format: 637390333
Labeler code: 63739
Product ID: 63739-333_c0f884b5-0f4e-520f-e053-2995a90adba0
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Ondansetron
Dosage form: TABLET
Route: ORAL
Labeler: McKesson Corporation dba SKY Packaging
Application: ANDA077851
Marketing category: ANDA
Marketing start: 2018-07-11
Marketing end: 0000-00-00
Substance: ONDANSETRON HYDROCHLORIDE
Active strength: 8 mg/1
Pharmacologic classes: Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63739-333-10	2020-07-22	C162847	48780-1	ab0e2407-3199-f274-e053-dbdaa90a6471	7bbac33c-f8a7-4d61-96a1-defd1bc13dc5

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-333-10	EA - Each	63739-333	dd8b793b-1080-420c-821e-759599ef9d40	1	2019-08-06

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
NMH84OZK2B	ONDANSETRON HYDROCHLORIDE	103639-04-9	ONDANSETRON HYDROCHLORIDE
4AF302ESOS	ONDANSETRON	99614-02-5	Ondansetron

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-333-10	63739033310	10 BLISTER PACK in 1 BOX (63739-333-10) > 10 TABLET in 1 BLISTER PACK	10 blister pack	2019-07-24	0000-00-00	No	No	Current