Ranitidine - Ranitidine
Navigation: NDC > Supplier starting with: I > IVAX PHARMACEUTICALS, INC.| Field | Value |
|---|---|
| NDC Code: | 0172-4357 |
| Proprietary Name: | Ranitidine |
| Suffix: | |
| Non-Proprietary Name: | Ranitidine |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 12-09-1997 |
| Category Name: | ANDA |
| Application Number: | ANDA075165 |
| Labeler: | IVAX PHARMACEUTICALS, INC. |
| Substance Name: | RANITIDINE HYDROCHLORIDE |
| Active Numerator Strength: | 150 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
| DEA Schedule: |