Halobetasol Propionate

Product NDC
72162-2258
11-digit product format
721622258
Labeler code
72162
Product ID
72162-2258_f3298f27-cc86-4166-828b-8a751617b18c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Halobetasol Propionate
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Application
ANDA077109
Marketing category
ANDA
Marketing start
2005-06-14
Substance
HALOBETASOL PROPIONATE
Active strength
.5 mg/g
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
91A0K1TY3ZHALOBETASOL PROPIONATE66852-54-8HALOBETASOL PROPIONATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-2258-2721622258021 TUBE in 1 CARTON (72162-2258-2) / 50 g in 1 TUBE1 tube2018-02-21NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Halobetasol Propionate Ointment, 0.05% For Dermatological Use Only. Not for Ophthalmic Use. Rx OnlyBryant Ranch Prepack2024-05-29HUMAN PRESCRIPTION DRUG LABEL101