Product NDC: | 57344-150 |
Proprietary Name: | Cold Multi-Symptom Daytime Nighttime |
Non Proprietary Name: | Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride |
Active Ingredient(s): | & nbsp; Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57344-150 |
Labeler Name: | AAA Pharmaceutical, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121228 |
Package NDC: | 57344-150-02 |
Package Description: | 1 KIT in 1 CARTON (57344-150-02) * 12 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK |
NDC Code | 57344-150-02 |
Proprietary Name | Cold Multi-Symptom Daytime Nighttime |
Package Description | 1 KIT in 1 CARTON (57344-150-02) * 12 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK |
Product NDC | 57344-150 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20121228 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | AAA Pharmaceutical, Inc. |
Substance Name | |
Strength Number | |
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