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Alka Seltzer
Alka Seltzer - 53666-100-10 - (ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE)
Drug Information of Alka Seltzer
| Product NDC: | 53666-100 |
| Proprietary Name: | Alka Seltzer |
| Non Proprietary Name: | ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE |
| Active Ingredient(s): | 1000; 325; 1916 mg/1; mg/1; mg/1 & nbsp; ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EFFERVESCENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alka Seltzer
| Product NDC: | 53666-100 |
| Labeler Name: | Salimex, S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121010 |
Package Information of Alka Seltzer
| Package NDC: | 53666-100-10 |
| Package Description: | 100 TABLET, EFFERVESCENT in 1 BOX (53666-100-10) |
NDC Information of Alka Seltzer
| NDC Code | 53666-100-10 |
| Proprietary Name | Alka Seltzer |
| Package Description | 100 TABLET, EFFERVESCENT in 1 BOX (53666-100-10) |
| Product NDC | 53666-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE |
| Dosage Form Name | TABLET, EFFERVESCENT |
| Route Name | ORAL |
| Start Marketing Date | 20121010 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Salimex, S.A. |
| Substance Name | ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE |
| Strength Number | 1000; 325; 1916 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
