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| Product NDC Code | 72785-0001 | ||||
|---|---|---|---|---|---|
| Drug Name | Ranitidine hydrochloride |
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| Type | Generic | ||||
| Pharm Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
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| Active Ingredients |
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| Route | INTRAMUSCULAR, INTRAVENOUS | ||||
| Dosage Form | INJECTION, SOLUTION | ||||
| RxCUI drug identifier | 312772 | ||||
| Application Number | ANDA091534 | ||||
| Labeler Name | Zydus Lifesciences Limited | ||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Spl product data elements
Usually a list of ingredients in a drug product.Ranitidine Hydrochloride ranitidine hydrochloride RANITIDINE HYDROCHLORIDE RANITIDINE PHENOL POTASSIUM PHOSPHATE, MONOBASIC SODIUM PHOSPHATE, DIBASIC colorless to yellow
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.PRINCIPAL DISPLAY PANEL - 40 mL Vial Container Label NDC 72785-0001-1 Ranitidine Injection USP 1000 mg/40 mL (25 mg/mL*) 40-mL Pharmacy Bulk package – Not for Direct Infusion Sterile Rx only Zydus pharmaceuticals PRINCIPAL DISPLAY PANEL - 40 mL Vial Carton Label NDC 72785-0001-1 Ranitidine Injection USP 1000 mg/40 mL (25 mg/mL*) 40-mL Pharmacy Bulk Package – Not for Direct Infusion Sterile Rx only Zydus pharmaceuticals vial label carton label
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API