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Alclometasone Dipropionate
Alclometasone Dipropionate - 0168-0264-45 - (alclometasone dipropionate)
Drug Information of Alclometasone Dipropionate
| Product NDC: | 0168-0264 |
| Proprietary Name: | Alclometasone Dipropionate |
| Non Proprietary Name: | alclometasone dipropionate |
| Active Ingredient(s): | .5 mg/g & nbsp; alclometasone dipropionate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alclometasone Dipropionate
| Product NDC: | 0168-0264 |
| Labeler Name: | E. Fougera & Co., a division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076884 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050718 |
Package Information of Alclometasone Dipropionate
| Package NDC: | 0168-0264-45 |
| Package Description: | 1 TUBE in 1 CARTON (0168-0264-45) > 45 g in 1 TUBE |
NDC Information of Alclometasone Dipropionate
| NDC Code | 0168-0264-45 |
| Proprietary Name | Alclometasone Dipropionate |
| Package Description | 1 TUBE in 1 CARTON (0168-0264-45) > 45 g in 1 TUBE |
| Product NDC | 0168-0264 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | alclometasone dipropionate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20050718 |
| Marketing Category Name | ANDA |
| Labeler Name | E. Fougera & Co., a division of Fougera Pharmaceuticals Inc. |
| Substance Name | ALCLOMETASONE DIPROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
