Product NDC: | 16590-993 |
Proprietary Name: | MOMETASONE FUROATE |
Non Proprietary Name: | MOMETASONE FUROATE |
Active Ingredient(s): | 1 mg/g & nbsp; MOMETASONE FUROATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-993 |
Labeler Name: | STAT RX USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077447 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060823 |
Package NDC: | 16590-993-15 |
Package Description: | 15 g in 1 TUBE (16590-993-15) |
NDC Code | 16590-993-15 |
Proprietary Name | MOMETASONE FUROATE |
Package Description | 15 g in 1 TUBE (16590-993-15) |
Product NDC | 16590-993 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | MOMETASONE FUROATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20060823 |
Marketing Category Name | ANDA |
Labeler Name | STAT RX USA LLC |
Substance Name | MOMETASONE FUROATE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes |