Tovet Foam (Emollient Formulation)

Product NDC: 43538-953
11-digit product format: 435380953
Labeler code: 43538
Product ID: 43538-953_b864bf0c-c4a6-4f98-8cee-1f6377d9e685
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: CLOBETASOL PROPIONATE
Dosage form: KIT
Labeler: Medimetriks Pharmaceuticals, Inc.
Application: ANDA201402
Marketing category: ANDA
Marketing start: 2013-02-01
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
43538-953-10	2021-12-07	C162847	48780-1	c7ccaba7-20e5-fd44-e053-dadaa90aa01b	These highlights do not include all the information needed to use TOVET (CLOBETASOL PROPIONATE) FOAM (EMULSION) safely and effectively. See full prescribing information for TOVET (CLOBETASOL PROPIONATE) FOAM (EMULSION). TOVET ® (CLOBETASOL PROPIONATE) foam, 0.05% (Emollient Formulation) For topical use Initial U.S. Approval: 1985
43538-953-10	2021-07-23	C162847	48780-1	c7ccaba7-20e5-fd44-e053-dadaa90aa01b	These highlights do not include all the information needed to use TOVET (CLOBETASOL PROPIONATE) FOAM (EMULSION) safely and effectively. See full prescribing information for TOVET (CLOBETASOL PROPIONATE) FOAM (EMULSION). TOVET ® (CLOBETASOL PROPIONATE) foam, 0.05% (Emollient Formulation) For topical use Initial U.S. Approval: 1985

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
43538-953-10	GM - Gram	43538-953	e54e730b-70f8-4124-a720-3fa894487fdb	1	2019-12-10

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
43538-953-10	43538095310	1 KIT in 1 CARTON (43538-953-10) * 100 g in 1 CANISTER * 255 g in 1 TUBE	1 kit	2019-08-01	0000-00-00	No	No	Current