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Methscopolamine Bromide
Methscopolamine Bromide - 0168-0483-60 - (methscopolamine bromide)
Drug Information of Methscopolamine Bromide
| Product NDC: | 0168-0483 |
| Proprietary Name: | Methscopolamine Bromide |
| Non Proprietary Name: | methscopolamine bromide |
| Active Ingredient(s): | 5 mg/1 & nbsp; methscopolamine bromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methscopolamine Bromide
| Product NDC: | 0168-0483 |
| Labeler Name: | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA008848 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20110727 |
Package Information of Methscopolamine Bromide
| Package NDC: | 0168-0483-60 |
| Package Description: | 5 BLISTER PACK in 1 BOX (0168-0483-60) > 12 TABLET in 1 BLISTER PACK |
NDC Information of Methscopolamine Bromide
| NDC Code | 0168-0483-60 |
| Proprietary Name | Methscopolamine Bromide |
| Package Description | 5 BLISTER PACK in 1 BOX (0168-0483-60) > 12 TABLET in 1 BLISTER PACK |
| Product NDC | 0168-0483 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methscopolamine bromide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110727 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Substance Name | METHSCOPOLAMINE BROMIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
