Product NDC: | 0085-0575 |
Proprietary Name: | DIPROLENE |
Non Proprietary Name: | betamethasone dipropionate |
Active Ingredient(s): | .5 mg/g & nbsp; betamethasone dipropionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0085-0575 |
Labeler Name: | Merck Sharp & Dohme Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018741 |
Marketing Category: | NDA |
Start Marketing Date: | 19830727 |
Package NDC: | 0085-0575-02 |
Package Description: | 1 TUBE in 1 BOX (0085-0575-02) > 15 g in 1 TUBE |
NDC Code | 0085-0575-02 |
Proprietary Name | DIPROLENE |
Package Description | 1 TUBE in 1 BOX (0085-0575-02) > 15 g in 1 TUBE |
Product NDC | 0085-0575 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | betamethasone dipropionate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 19830727 |
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] |