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Acid reducer
Acid reducer - 41268-141-65 - (Famotidine)
Drug Information of Acid reducer
| Product NDC: | 41268-141 |
| Proprietary Name: | Acid reducer |
| Non Proprietary Name: | Famotidine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Famotidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acid reducer
| Product NDC: | 41268-141 |
| Labeler Name: | Hannaford Brothers Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075400 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100203 |
Package Information of Acid reducer
| Package NDC: | 41268-141-65 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (41268-141-65) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Acid reducer
| NDC Code | 41268-141-65 |
| Proprietary Name | Acid reducer |
| Package Description | 3 BLISTER PACK in 1 CARTON (41268-141-65) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 41268-141 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100203 |
| Marketing Category Name | ANDA |
| Labeler Name | Hannaford Brothers Company |
| Substance Name | FAMOTIDINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
