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Glycopyrrolate
Glycopyrrolate - 64376-601-31 - (Glycopyrrolate)
Drug Information of Glycopyrrolate
| Product NDC: | 64376-601 |
| 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: | 64376-601 |
| Labeler Name: | Boca Pharmacal, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090020 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111019 |
Package Information of Glycopyrrolate
| Package NDC: | 64376-601-31 |
| Package Description: | 30 TABLET in 1 BOTTLE (64376-601-31) |
NDC Information of Glycopyrrolate
| NDC Code | 64376-601-31 |
| Proprietary Name | Glycopyrrolate |
| Package Description | 30 TABLET in 1 BOTTLE (64376-601-31) |
| Product NDC | 64376-601 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Glycopyrrolate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111019 |
| Marketing Category Name | ANDA |
| Labeler Name | Boca Pharmacal, Inc. |
| Substance Name | GLYCOPYRROLATE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
