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Carbinoxamine Maleate
Carbinoxamine Maleate - 51991-333-01 - (carbinoxamine maleate)
Drug Information of Carbinoxamine Maleate
| Product NDC: | 51991-333 |
| Proprietary Name: | Carbinoxamine Maleate |
| Non Proprietary Name: | carbinoxamine maleate |
| Active Ingredient(s): | 4 mg/1 & nbsp; carbinoxamine maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Carbinoxamine Maleate
| Product NDC: | 51991-333 |
| Labeler Name: | Breckenridge Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040442 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121210 |
Package Information of Carbinoxamine Maleate
| Package NDC: | 51991-333-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (51991-333-01) |
NDC Information of Carbinoxamine Maleate
| NDC Code | 51991-333-01 |
| Proprietary Name | Carbinoxamine Maleate |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (51991-333-01) |
| Product NDC | 51991-333 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | carbinoxamine maleate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121210 |
| Marketing Category Name | ANDA |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| Substance Name | CARBINOXAMINE MALEATE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
