Ultravate

Product NDC
10631-103
11-digit product format
106310103
Labeler code
10631
Product ID
10631-103_cd9a3fc1-f9e4-4ab7-9c75-50ab9c65e270
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
halobetasol propionate
Dosage form
CREAM
Route
TOPICAL
Labeler
Ranbaxy Laboratories Inc.
Application
NDA019967
Marketing category
NDA
Marketing start
2009-03-16
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10631-103-15GM - Gram10631-103b38fad98-ff68-479a-9146-f6b5cee5cfce12012-07-24
10631-103-50GM - Gram10631-1032b76c8e6-88b9-4f46-9a66-34bbb82bd29c12012-07-24