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Cold Multi-Symptom Daytime Rapid Release
Cold Multi-Symptom Daytime Rapid Release - 41163-560-08 - (Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr)
Drug Information of Cold Multi-Symptom Daytime Rapid Release
| Product NDC: | 41163-560 |
| Proprietary Name: | Cold Multi-Symptom Daytime Rapid Release |
| Non Proprietary Name: | Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr |
| Active Ingredient(s): | 325; 10; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cold Multi-Symptom Daytime Rapid Release
| Product NDC: | 41163-560 |
| Labeler Name: | SUPERVALU INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080329 |
Package Information of Cold Multi-Symptom Daytime Rapid Release
| Package NDC: | 41163-560-08 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (41163-560-08) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Cold Multi-Symptom Daytime Rapid Release
| NDC Code | 41163-560-08 |
| Proprietary Name | Cold Multi-Symptom Daytime Rapid Release |
| Package Description | 1 BLISTER PACK in 1 CARTON (41163-560-08) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 41163-560 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20080329 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SUPERVALU INC. |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
