Product NDC: | 51991-334 |
Proprietary Name: | Carbinoxamine Maleate |
Non Proprietary Name: | carbinoxamine maleate |
Active Ingredient(s): | 4 mg/5mL & nbsp; carbinoxamine maleate |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51991-334 |
Labeler Name: | Breckenridge Pharmaceutical, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040458 |
Marketing Category: | ANDA |
Start Marketing Date: | 20121210 |
Package NDC: | 51991-334-16 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (51991-334-16) |
NDC Code | 51991-334-16 |
Proprietary Name | Carbinoxamine Maleate |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (51991-334-16) |
Product NDC | 51991-334 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | carbinoxamine maleate |
Dosage Form Name | SYRUP |
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/5mL |
Pharmaceutical Classes |