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Arbinoxa
Arbinoxa - 63717-871-16 - (Carbinoxamine maleate)
Drug Information of Arbinoxa
| Product NDC: | 63717-871 |
| Proprietary Name: | Arbinoxa |
| Non Proprietary Name: | Carbinoxamine maleate |
| Active Ingredient(s): | .8 mg/mL & nbsp; Carbinoxamine maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arbinoxa
| Product NDC: | 63717-871 |
| Labeler Name: | Hawthorn Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090418 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110401 |
Package Information of Arbinoxa
| Package NDC: | 63717-871-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (63717-871-16) |
NDC Information of Arbinoxa
| NDC Code | 63717-871-16 |
| Proprietary Name | Arbinoxa |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (63717-871-16) |
| Product NDC | 63717-871 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carbinoxamine maleate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | ANDA |
| Labeler Name | Hawthorn Pharmaceuticals, Inc. |
| Substance Name | CARBINOXAMINE MALEATE |
| Strength Number | .8 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
