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Robinul
Robinul - 0641-6105-25 - (Robinul)
Drug Information of Robinul
| Product NDC: | 0641-6105 |
| Proprietary Name: | Robinul |
| Non Proprietary Name: | Robinul |
| Active Ingredient(s): | .2 mg/mL & nbsp; Robinul |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Robinul
| Product NDC: | 0641-6105 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017558 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19750206 |
Package Information of Robinul
| Package NDC: | 0641-6105-25 |
| Package Description: | 25 VIAL in 1 CARTON (0641-6105-25) > 2 mL in 1 VIAL (0641-6105-01) |
NDC Information of Robinul
| NDC Code | 0641-6105-25 |
| Proprietary Name | Robinul |
| Package Description | 25 VIAL in 1 CARTON (0641-6105-25) > 2 mL in 1 VIAL (0641-6105-01) |
| Product NDC | 0641-6105 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Robinul |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19750206 |
| Marketing Category Name | NDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | GLYCOPYRROLATE |
| Strength Number | .2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
