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acid reducer
acid reducer - 42507-141-72 - (Famotidine)
Drug Information of acid reducer
| Product NDC: | 42507-141 |
| 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: | 42507-141 |
| Labeler Name: | HyVee Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075400 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091019 |
Package Information of acid reducer
| Package NDC: | 42507-141-72 |
| Package Description: | 1 BOTTLE in 1 CARTON (42507-141-72) > 60 TABLET in 1 BOTTLE |
NDC Information of acid reducer
| NDC Code | 42507-141-72 |
| Proprietary Name | acid reducer |
| Package Description | 1 BOTTLE in 1 CARTON (42507-141-72) > 60 TABLET in 1 BOTTLE |
| Product NDC | 42507-141 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091019 |
| Marketing Category Name | ANDA |
| Labeler Name | HyVee Inc |
| Substance Name | FAMOTIDINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
