DIPROLENE - 0085-0962-01 - (betamethasone dipropionate)

Alphabetical Index


Drug Information of DIPROLENE

Product NDC: 0085-0962
Proprietary Name: DIPROLENE
Non Proprietary Name: betamethasone dipropionate
Active Ingredient(s): .5    mg/g & nbsp;   betamethasone dipropionate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of DIPROLENE

Product NDC: 0085-0962
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019716
Marketing Category: NDA
Start Marketing Date: 19880801

Package Information of DIPROLENE

Package NDC: 0085-0962-01
Package Description: 1 BOTTLE, PLASTIC in 1 BOX (0085-0962-01) > 29 g in 1 BOTTLE, PLASTIC

NDC Information of DIPROLENE

NDC Code 0085-0962-01
Proprietary Name DIPROLENE
Package Description 1 BOTTLE, PLASTIC in 1 BOX (0085-0962-01) > 29 g in 1 BOTTLE, PLASTIC
Product NDC 0085-0962
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name betamethasone dipropionate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 19880801
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name BETAMETHASONE DIPROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of DIPROLENE


General Information