Product NDC: | 57344-158 |
Proprietary Name: | Chlorpheniramine Maleate, Phenylephrine Hydrochloride |
Non Proprietary Name: | CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient(s): | 4; 10 mg/1; mg/1 & nbsp; CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57344-158 |
Labeler Name: | AAA Pharmaceutical, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121222 |
Package NDC: | 57344-158-02 |
Package Description: | 1 BLISTER PACK in 1 CARTON (57344-158-02) > 24 TABLET, COATED in 1 BLISTER PACK |
NDC Code | 57344-158-02 |
Proprietary Name | Chlorpheniramine Maleate, Phenylephrine Hydrochloride |
Package Description | 1 BLISTER PACK in 1 CARTON (57344-158-02) > 24 TABLET, COATED in 1 BLISTER PACK |
Product NDC | 57344-158 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20121222 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | AAA Pharmaceutical, Inc. |
Substance Name | CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 4; 10 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |