Product NDC: | 0054-4721 |
Proprietary Name: | Propantheline Bromide |
Non Proprietary Name: | Propantheline Bromide |
Active Ingredient(s): | 15 mg/1 & nbsp; Propantheline Bromide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-4721 |
Labeler Name: | Roxane Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA080927 |
Marketing Category: | ANDA |
Start Marketing Date: | 19811214 |
Package NDC: | 0054-4721-25 |
Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0054-4721-25) |
NDC Code | 0054-4721-25 |
Proprietary Name | Propantheline Bromide |
Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0054-4721-25) |
Product NDC | 0054-4721 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Propantheline Bromide |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19811214 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc. |
Substance Name | PROPANTHELINE BROMIDE |
Strength Number | 15 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |