Home
>
National Drug Code (NDC)
>
glycopyrrolate
glycopyrrolate - 0677-1932-01 - (glycopyrrolate)
Drug Information of glycopyrrolate
| Product NDC: | 0677-1932 |
| Proprietary Name: | glycopyrrolate |
| Non Proprietary Name: | glycopyrrolate |
| Active Ingredient(s): | 2 mg/1 & nbsp; glycopyrrolate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of glycopyrrolate
| Product NDC: | 0677-1932 |
| Labeler Name: | United Research Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012827 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20050113 |
Package Information of glycopyrrolate
| Package NDC: | 0677-1932-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0677-1932-01) |
NDC Information of glycopyrrolate
| NDC Code | 0677-1932-01 |
| Proprietary Name | glycopyrrolate |
| Package Description | 100 TABLET in 1 BOTTLE (0677-1932-01) |
| Product NDC | 0677-1932 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | glycopyrrolate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050113 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | United Research Laboratories, Inc. |
| Substance Name | GLYCOPYRROLATE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
