Ranitidine - Ranitidine
Navigation: NDC > Supplier starting with: S > SUNMARK| Field | Value |
|---|---|
| NDC Code: | 49348-473 |
| Proprietary Name: | Ranitidine |
| Suffix: | |
| Non-Proprietary Name: | Ranitidine |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 20-09-2013 |
| Category Name: | ANDA |
| Application Number: | ANDA201745 |
| Labeler: | SUNMARK |
| Substance Name: | RANITIDINE HYDROCHLORIDE |
| Active Numerator Strength: | 75 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | |
| DEA Schedule: |