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Robinul
Robinul - 59630-200-10 - (Glycopyrrolate)
Drug Information of Robinul
| Product NDC: | 59630-200 |
| Proprietary Name: | Robinul |
| 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 Robinul
| Product NDC: | 59630-200 |
| Labeler Name: | Shionogi Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012827 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19610328 |
Package Information of Robinul
| Package NDC: | 59630-200-10 |
| Package Description: | 100 TABLET in 1 BOTTLE (59630-200-10) |
NDC Information of Robinul
| NDC Code | 59630-200-10 |
| Proprietary Name | Robinul |
| Package Description | 100 TABLET in 1 BOTTLE (59630-200-10) |
| Product NDC | 59630-200 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Glycopyrrolate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19610328 |
| Marketing Category Name | NDA |
| Labeler Name | Shionogi Inc. |
| Substance Name | GLYCOPYRROLATE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
