Product NDC: | 64376-604 |
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) |
Product NDC: | 64376-604 |
Labeler Name: | Boca Pharmacal, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040624 |
Marketing Category: | ANDA |
Start Marketing Date: | 20061228 |
Package NDC: | 64376-604-61 |
Package Description: | 60 TABLET in 1 BOTTLE (64376-604-61) |
NDC Code | 64376-604-61 |
Proprietary Name | Methscopolamine Bromide |
Package Description | 60 TABLET in 1 BOTTLE (64376-604-61) |
Product NDC | 64376-604 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Methscopolamine Bromide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20061228 |
Marketing Category Name | ANDA |
Labeler Name | Boca Pharmacal, Inc. |
Substance Name | METHSCOPOLAMINE BROMIDE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |