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Famotidine
Famotidine - 49035-128-90 - (Famotidine)
Drug Information of Famotidine
| Product NDC: | 49035-128 |
| Proprietary Name: | Famotidine |
| 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 Famotidine
| Product NDC: | 49035-128 |
| Labeler Name: | EQUATE (Walmart Stores, Inc.) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077146 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121218 |
Package Information of Famotidine
| Package NDC: | 49035-128-90 |
| Package Description: | 1 BOTTLE in 1 BOX (49035-128-90) > 90 TABLET in 1 BOTTLE |
NDC Information of Famotidine
| NDC Code | 49035-128-90 |
| Proprietary Name | Famotidine |
| Package Description | 1 BOTTLE in 1 BOX (49035-128-90) > 90 TABLET in 1 BOTTLE |
| Product NDC | 49035-128 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121218 |
| Marketing Category Name | ANDA |
| Labeler Name | EQUATE (Walmart Stores, Inc.) |
| Substance Name | FAMOTIDINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
