NDC Labeler Sun Pharmaceutical Industries Limited
Sun Pharmaceutical Industries Limited labeler's code is 54907. The labeler has 9 products that have an assigned National Drug Code.
NDC | Proprietary Name | Non-Proprietary Name | Dosage Form | Route Name | Product Type | Status |
---|---|---|---|---|---|---|
70095-017 | Theophylline | Theophylline | Tablet, Extended Release | Oral | Human Prescription Drug | ACTIVE |
70095-018 | Theophylline | Theophylline | Tablet, Extended Release | Oral | Human Prescription Drug | ACTIVE |
70095-019 | Bisoprolol Fumarate | Bisoprolol Fumarate | Tablet, Film Coated | Oral | Human Prescription Drug | ACTIVE |
70095-020 | Bisoprolol Fumarate | Bisoprolol Fumarate | Tablet, Film Coated | Oral | Human Prescription Drug | ACTIVE |
70095-024 | Pantoprazole Sodium | Pantoprazole Sodium | Injection, Powder, Lyophilized, For Solution | Intravenous | Human Prescription Drug | ACTIVE |
70095-025 | Azithromycin Monohydrate | Azithromycin Monohydrate | Injection, Powder, Lyophilized, For Solution | Intravenous | Human Prescription Drug | ACTIVE |
70095-026 | Desmopressin Acetate | Desmopressin Acetate | Injection, Solution | Intravenous; Subcutaneous | Human Prescription Drug | ACTIVE |
70095-031 | Desmopressin Acetate | Desmopressin Acetate | Injection, Solution | Intravenous; Subcutaneous | Human Prescription Drug | ACTIVE |
70095-050 | Sodium Bicarbonate | Sodium Bicarbonate | Injection, Solution | Intravenous | Human Prescription Drug | ACTIVE |