Rx Act Heartburn Prevention - Famotidine
Navigation: NDC > Supplier starting with: H > H E B| Field | Value |
|---|---|
| NDC Code: | 37808-194 |
| Proprietary Name: | Rx Act Heartburn Prevention |
| Suffix: | maximum strength |
| Non-Proprietary Name: | Famotidine |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 28-09-2006 |
| Category Name: | ANDA |
| Application Number: | ANDA077351 |
| Labeler: | H E B |
| Substance Name: | FAMOTIDINE |
| Active Numerator Strength: | 20 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | |
| DEA Schedule: |