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SunMark Acid Reducer
SunMark Acid Reducer - 49348-817-09 - (Famotidine)
Drug Information of SunMark Acid Reducer
| Product NDC: | 49348-817 |
| Proprietary Name: | SunMark Acid Reducer |
| Non Proprietary Name: | Famotidine |
| Active Ingredient(s): | 20 mg/1 & nbsp; Famotidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SunMark Acid Reducer
| Product NDC: | 49348-817 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077351 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070618 |
Package Information of SunMark Acid Reducer
| Package NDC: | 49348-817-09 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-817-09) > 50 TABLET in 1 BOTTLE |
NDC Information of SunMark Acid Reducer
| NDC Code | 49348-817-09 |
| Proprietary Name | SunMark Acid Reducer |
| Package Description | 1 BOTTLE in 1 CARTON (49348-817-09) > 50 TABLET in 1 BOTTLE |
| Product NDC | 49348-817 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070618 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | FAMOTIDINE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
