Ranitidine - Ranitidine Hydrochloride
Navigation: NDC > Supplier starting with: A > AUROBINDO PHARMA LIMITED| Field | Value |
|---|---|
| NDC Code: | 65862-431 |
| Proprietary Name: | Ranitidine |
| Suffix: | |
| Non-Proprietary Name: | Ranitidine Hydrochloride |
| Dosage Form: | SYRUP |
| Method: | ORAL |
| Original Marketing Date: | 28-07-2010 |
| Category Name: | ANDA |
| Application Number: | ANDA090623 |
| Labeler: | AUROBINDO PHARMA LIMITED |
| Substance Name: | RANITIDINE HYDROCHLORIDE |
| Active Numerator Strength: | 15 |
| Active Ingredient Unit: | mg/mL |
| Pharm Classes: | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
| DEA Schedule: |