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Major Heartburn Relief
Major Heartburn Relief - 0904-5780-17 - (Famotidine)
Drug Information of Major Heartburn Relief
| Product NDC: | 0904-5780 |
| Proprietary Name: | Major Heartburn Relief |
| 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 Major Heartburn Relief
| Product NDC: | 0904-5780 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077351 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060929 |
Package Information of Major Heartburn Relief
| Package NDC: | 0904-5780-17 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (0904-5780-17) > 5 TABLET in 1 BLISTER PACK |
NDC Information of Major Heartburn Relief
| NDC Code | 0904-5780-17 |
| Proprietary Name | Major Heartburn Relief |
| Package Description | 5 BLISTER PACK in 1 CARTON (0904-5780-17) > 5 TABLET in 1 BLISTER PACK |
| Product NDC | 0904-5780 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060929 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | FAMOTIDINE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
