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FAMOTIDINE
FAMOTIDINE - 64679-374-09 - (FAMOTIDINE)
Drug Information of FAMOTIDINE
| Product NDC: | 64679-374 |
| Proprietary Name: | FAMOTIDINE |
| 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 FAMOTIDINE
| Product NDC: | 64679-374 |
| Labeler Name: | WOCKHARDT USA LLC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090837 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100806 |
Package Information of FAMOTIDINE
| Package NDC: | 64679-374-09 |
| Package Description: | 6500 TABLET in 1 DRUM (64679-374-09) |
NDC Information of FAMOTIDINE
| NDC Code | 64679-374-09 |
| Proprietary Name | FAMOTIDINE |
| Package Description | 6500 TABLET in 1 DRUM (64679-374-09) |
| Product NDC | 64679-374 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | FAMOTIDINE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100806 |
| Marketing Category Name | ANDA |
| Labeler Name | WOCKHARDT USA LLC. |
| Substance Name | FAMOTIDINE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
