Ranitidine Hydrochloride - Ranitidine Hydrochloride
Navigation: NDC > Supplier starting with: S > SANDOZ INC| Field | Value |
|---|---|
| NDC Code: | 0781-1884 |
| Proprietary Name: | Ranitidine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Ranitidine Hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 29-08-1997 |
| Category Name: | ANDA |
| Application Number: | ANDA074467 |
| Labeler: | SANDOZ INC |
| Substance Name: | RANITIDINE HYDROCHLORIDE |
| Active Numerator Strength: | 300 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
| DEA Schedule: |