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Glycopyrrolate
Glycopyrrolate - 49884-065-01 - (glycopyrrolate)
Drug Information of Glycopyrrolate
| Product NDC: | 49884-065 |
| Proprietary Name: | Glycopyrrolate |
| Non Proprietary Name: | glycopyrrolate |
| Active Ingredient(s): | 1 mg/1 & nbsp; glycopyrrolate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glycopyrrolate
| Product NDC: | 49884-065 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040653 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060926 |
Package Information of Glycopyrrolate
| Package NDC: | 49884-065-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (49884-065-01) |
NDC Information of Glycopyrrolate
| NDC Code | 49884-065-01 |
| Proprietary Name | Glycopyrrolate |
| Package Description | 100 TABLET in 1 BOTTLE (49884-065-01) |
| Product NDC | 49884-065 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | glycopyrrolate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060926 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | GLYCOPYRROLATE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
