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FAMOTIDINE
FAMOTIDINE - 0172-2662-48 - (Famotidine)
Drug Information of FAMOTIDINE
| Product NDC: | 0172-2662 |
| 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: | 0172-2662 |
| Labeler Name: | IVAX Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075512 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100218 |
Package Information of FAMOTIDINE
| Package NDC: | 0172-2662-48 |
| Package Description: | 50 BLISTER PACK in 1 CARTON (0172-2662-48) > 1 TABLET in 1 BLISTER PACK (0172-2662-00) |
NDC Information of FAMOTIDINE
| NDC Code | 0172-2662-48 |
| Proprietary Name | FAMOTIDINE |
| Package Description | 50 BLISTER PACK in 1 CARTON (0172-2662-48) > 1 TABLET in 1 BLISTER PACK (0172-2662-00) |
| Product NDC | 0172-2662 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100218 |
| Marketing Category Name | ANDA |
| Labeler Name | IVAX Pharmaceuticals, Inc. |
| Substance Name | FAMOTIDINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
