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Alka-Seltzer Plus
Alka-Seltzer Plus - 0280-1175-48 - (Diphenhydramine Hydrochloride)
Drug Information of Alka-Seltzer Plus
| Product NDC: | 0280-1175 |
| Proprietary Name: | Alka-Seltzer Plus |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alka-Seltzer Plus
| Product NDC: | 0280-1175 |
| Labeler Name: | Bayer HealthCare LLC, Consumer Care |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111107 |
Package Information of Alka-Seltzer Plus
| Package NDC: | 0280-1175-48 |
| Package Description: | 4 BLISTER PACK in 1 CARTON (0280-1175-48) > 12 TABLET in 1 BLISTER PACK |
NDC Information of Alka-Seltzer Plus
| NDC Code | 0280-1175-48 |
| Proprietary Name | Alka-Seltzer Plus |
| Package Description | 4 BLISTER PACK in 1 CARTON (0280-1175-48) > 12 TABLET in 1 BLISTER PACK |
| Product NDC | 0280-1175 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111107 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bayer HealthCare LLC, Consumer Care |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
