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Alka-Seltzer Plus
Alka-Seltzer Plus - 0280-7050-20 - (Acetaminophen, Chlorpheniramine maleate, Phenylephrine Hydrochloride, and Dextromethorphan hydrobromide)
Drug Information of Alka-Seltzer Plus
| Product NDC: | 0280-7050 |
| Proprietary Name: | Alka-Seltzer Plus |
| Non Proprietary Name: | Acetaminophen, Chlorpheniramine maleate, Phenylephrine Hydrochloride, and Dextromethorphan hydrobromide |
| Active Ingredient(s): | 250; 2; 10; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Chlorpheniramine maleate, Phenylephrine Hydrochloride, and Dextromethorphan hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EFFERVESCENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alka-Seltzer Plus
| Product NDC: | 0280-7050 |
| Labeler Name: | Bayer Corporation Consumer Care Division |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100801 |
Package Information of Alka-Seltzer Plus
| Package NDC: | 0280-7050-20 |
| Package Description: | 1 POUCH in 1 CARTON (0280-7050-20) > 20 TABLET, EFFERVESCENT in 1 POUCH |
NDC Information of Alka-Seltzer Plus
| NDC Code | 0280-7050-20 |
| Proprietary Name | Alka-Seltzer Plus |
| Package Description | 1 POUCH in 1 CARTON (0280-7050-20) > 20 TABLET, EFFERVESCENT in 1 POUCH |
| Product NDC | 0280-7050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Chlorpheniramine maleate, Phenylephrine Hydrochloride, and Dextromethorphan hydrobromide |
| Dosage Form Name | TABLET, EFFERVESCENT |
| Route Name | ORAL |
| Start Marketing Date | 20100801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bayer Corporation Consumer Care Division |
| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 250; 2; 10; 5 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
