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Cogentin
Cogentin - 76478-611-02 - (benztropine mesylate)
Drug Information of Cogentin
| Product NDC: | 76478-611 |
| Proprietary Name: | Cogentin |
| Non Proprietary Name: | benztropine mesylate |
| Active Ingredient(s): | 1 mg/mL & nbsp; benztropine mesylate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cogentin
| Product NDC: | 76478-611 |
| Labeler Name: | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012015 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19590805 |
Package Information of Cogentin
| Package NDC: | 76478-611-02 |
| Package Description: | 5 AMPULE in 1 CARTON (76478-611-02) > 2 mL in 1 AMPULE |
NDC Information of Cogentin
| NDC Code | 76478-611-02 |
| Proprietary Name | Cogentin |
| Package Description | 5 AMPULE in 1 CARTON (76478-611-02) > 2 mL in 1 AMPULE |
| Product NDC | 76478-611 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benztropine mesylate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19590805 |
| Marketing Category Name | NDA |
| Labeler Name | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
| Substance Name | BENZTROPINE MESYLATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA] |
