Halobetasol Propionate

Product NDC
51672-1322
11-digit product format
516721322
Labeler code
51672
Product ID
51672-1322_9e50ab82-0f41-4034-bce0-747380a3d735
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Halobetasol Propionate
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Taro Pharmaceuticals U.S.A., Inc.
Application
ANDA076994
Marketing category
ANDA
Marketing start
2004-12-16
Marketing end
0000-00-00
Substance
HALOBETASOL PROPIONATE
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51672-1322-1GM - Gram51672-1322a185d384-4e4d-472d-8f92-261d510653e312012-07-24
51672-1322-3GM - Gram51672-13226ae60970-13bd-479d-a4e4-833e2171630312012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-1322HALOBETASOL PROPIONATE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]5Legacy NDC20241211_1b3fd144-9ebd-46b0-b240-8bca47d101cd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51672-1322-1516721322011 TUBE in 1 CARTON (51672-1322-1) > 15 g in 1 TUBE1 tube2004-12-160000-00-00NoNoCurrent
51672-1322-3516721322031 TUBE in 1 CARTON (51672-1322-3) > 50 g in 1 TUBE1 tube2004-12-160000-00-00NoNoCurrent
51672-1322-5516721322055 g in 1 TUBE (51672-1322-5) 5 g2004-12-160000-00-00NoNoCurrent