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Sunmark Acid Reducer
Sunmark Acid Reducer - 49348-442-59 - (Famotidine)
Drug Information of Sunmark Acid Reducer
| Product NDC: | 49348-442 |
| Proprietary Name: | Sunmark Acid Reducer |
| Non Proprietary Name: | Famotidine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Famotidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark Acid Reducer
| Product NDC: | 49348-442 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075312 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030811 |
Package Information of Sunmark Acid Reducer
| Package NDC: | 49348-442-59 |
| Package Description: | 4 BLISTER PACK in 1 CARTON (49348-442-59) > 10 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Sunmark Acid Reducer
| NDC Code | 49348-442-59 |
| Proprietary Name | Sunmark Acid Reducer |
| Package Description | 4 BLISTER PACK in 1 CARTON (49348-442-59) > 10 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 49348-442 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030811 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | FAMOTIDINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
