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Benztropine Mesylate
Benztropine Mesylate - 0517-0785-05 - (Benztropine Mesylate)
Drug Information of Benztropine Mesylate
| Product NDC: | 0517-0785 |
| Proprietary Name: | Benztropine Mesylate |
| Non Proprietary Name: | Benztropine Mesylate |
| Active Ingredient(s): | 1 mg/mL & nbsp; Benztropine Mesylate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Benztropine Mesylate
| Product NDC: | 0517-0785 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091152 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110204 |
Package Information of Benztropine Mesylate
| Package NDC: | 0517-0785-05 |
| Package Description: | 5 VIAL, SINGLE-USE in 1 CARTON (0517-0785-05) > 2 mL in 1 VIAL, SINGLE-USE (0517-0785-01) |
NDC Information of Benztropine Mesylate
| NDC Code | 0517-0785-05 |
| Proprietary Name | Benztropine Mesylate |
| Package Description | 5 VIAL, SINGLE-USE in 1 CARTON (0517-0785-05) > 2 mL in 1 VIAL, SINGLE-USE (0517-0785-01) |
| Product NDC | 0517-0785 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Benztropine Mesylate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20110204 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, 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] |
