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Day and Night Cold
Day and Night Cold - 57344-147-01 - (Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride)
Drug Information of Day and Night Cold
| Product NDC: | 57344-147 |
| Proprietary Name: | Day and Night Cold |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride |
| Active Ingredient(s): | & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Day and Night Cold
| Product NDC: | 57344-147 |
| Labeler Name: | AAA Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121228 |
Package Information of Day and Night Cold
| Package NDC: | 57344-147-01 |
| Package Description: | 1 KIT in 1 CARTON (57344-147-01) * 10 TABLET, COATED in 1 BLISTER PACK * 10 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Day and Night Cold
| NDC Code | 57344-147-01 |
| Proprietary Name | Day and Night Cold |
| Package Description | 1 KIT in 1 CARTON (57344-147-01) * 10 TABLET, COATED in 1 BLISTER PACK * 10 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 57344-147 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, 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 | |
| Strength Unit | |
| Pharmaceutical Classes |
