Home
>
National Drug Code (NDC)
>
heartburn releif
heartburn releif - 0904-5529-52 - (Famotidine)
Drug Information of heartburn releif
| Product NDC: | 0904-5529 |
| Proprietary Name: | heartburn releif |
| 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 heartburn releif
| Product NDC: | 0904-5529 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075400 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090909 |
Package Information of heartburn releif
| Package NDC: | 0904-5529-52 |
| Package Description: | 1 BOTTLE in 1 CARTON (0904-5529-52) > 60 TABLET in 1 BOTTLE |
NDC Information of heartburn releif
| NDC Code | 0904-5529-52 |
| Proprietary Name | heartburn releif |
| Package Description | 1 BOTTLE in 1 CARTON (0904-5529-52) > 60 TABLET in 1 BOTTLE |
| Product NDC | 0904-5529 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090909 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | FAMOTIDINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
