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Glycopyrrolate
Glycopyrrolate - 0722-7097-01 - (Glycopyrrolate)
Drug Information of Glycopyrrolate
| Product NDC: | 0722-7097 |
| Proprietary Name: | Glycopyrrolate |
| Non Proprietary Name: | Glycopyrrolate |
| Active Ingredient(s): | 1.5 mg/1 & nbsp; Glycopyrrolate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glycopyrrolate
| Product NDC: | 0722-7097 |
| Labeler Name: | Nexgen Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091522 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120312 |
Package Information of Glycopyrrolate
| Package NDC: | 0722-7097-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0722-7097-01) |
NDC Information of Glycopyrrolate
| NDC Code | 0722-7097-01 |
| Proprietary Name | Glycopyrrolate |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0722-7097-01) |
| Product NDC | 0722-7097 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Glycopyrrolate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120312 |
| Marketing Category Name | ANDA |
| Labeler Name | Nexgen Pharma, Inc. |
| Substance Name | GLYCOPYRROLATE |
| Strength Number | 1.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
