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Alka-Seltzer Plus
Alka-Seltzer Plus - 0280-1435-20 - (Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, and Phenylephrine hydrochloride)
Drug Information of Alka-Seltzer Plus
| Product NDC: | 0280-1435 |
| Proprietary Name: | Alka-Seltzer Plus |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, and Phenylephrine hydrochloride |
| Active Ingredient(s): | 325; 10; 6.25; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, and Phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alka-Seltzer Plus
| Product NDC: | 0280-1435 |
| Labeler Name: | Bayer HealthCare LLC - Consumer Care |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120530 |
Package Information of Alka-Seltzer Plus
| Package NDC: | 0280-1435-20 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (0280-1435-20) > 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Alka-Seltzer Plus
| NDC Code | 0280-1435-20 |
| Proprietary Name | Alka-Seltzer Plus |
| Package Description | 1 BLISTER PACK in 1 CARTON (0280-1435-20) > 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 0280-1435 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, and Phenylephrine hydrochloride |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20120530 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bayer HealthCare LLC - Consumer Care |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 6.25; 5 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
