Betamethasone Dipropionate

Product NDC: 63739-996
11-digit product format: 637390996
Labeler code: 63739
Product ID: 63739-996_2e6365d8-cbee-42dd-b919-373edf1ce243
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: betamethasone dipropionate
Dosage form: OINTMENT
Route: TOPICAL
Labeler: McKesson Corporation
Application: ANDA206118
Marketing category: ANDA
Marketing start: 2020-03-12
Marketing end: 0000-00-00
Substance: BETAMETHASONE DIPROPIONATE
Active strength: 1 mg/g
Pharmacologic classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63739-996-65	2023-03-24	C162847	48780-1	f386c64a-3c92-0266-e053-dadaa90a7c1a	51530f90-6587-494d-8059-610820fa5d0b
63739-996-65	2023-01-30	C162847	48780-1	f386c64a-3c92-0266-e053-dadaa90a7c1a	51530f90-6587-494d-8059-610820fa5d0b

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-996-65	GM - Gram	63739-996	7548fe68-8af9-4545-af2b-3a10e126f537	1	2020-09-14

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
826Y60901U	BETAMETHASONE DIPROPIONATE	5593-20-4	BETAMETHASONE DIPROPIONATE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-996-65	63739099665	1 TUBE in 1 CARTON (63739-996-65) > 15 g in 1 TUBE	1 tube	2020-03-12	0000-00-00	No	No	Current