Product NDC: | 53666-403 |
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) |
Product NDC: | 53666-403 |
Labeler Name: | Salimex, S.A. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121010 |
Package NDC: | 53666-403-15 |
Package Description: | 150 BOX in 1 CASE (53666-403-15) > 12 TABLET, EFFERVESCENT in 1 BOX (53666-403-33) |
NDC Code | 53666-403-15 |
Proprietary Name | Alka Seltzer |
Package Description | 150 BOX in 1 CASE (53666-403-15) > 12 TABLET, EFFERVESCENT in 1 BOX (53666-403-33) |
Product NDC | 53666-403 |
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 |