Gemcitabine - Hydrochloride 1 g / 1 Injection 1 Vial, Single-Dose
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 71288-0114-50 |
|---|---|
| Product NDC | 71288-0114 |
| Generic Drug Name | Gemcitabine Hydrochloride |
| Brand Name | Gemcitabine |
| Manufacturer | Meitheal Pharmaceuticals Inc. |
| Strength | 1 g / 1 |
| Dosage Form | Injection |
| Drug Type | Intravenous |
| Package Quantity | 1 Vial, Single-Dose |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-114-50) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
| Active Ingredients | Gemcitabine Hydrochloride |
| Marketing Category | ANDA |
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NDC snapshot
Gemcitabine Hydrochloride 1 g / 1 Injection is tracked under NDC 71288-0114-50 and rolls up into product family 71288-0114. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 1 Vial, Single-Dose.
- Manufacturer: Meitheal Pharmaceuticals Inc..
- Dosage form: Injection.
- Family size: 1 indexed presentation.
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Official references
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Potential alternatives with matching presentation
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Gemcitabine - Hydrochloride 1 g / 1 Injection 1 Vial, Single-Dose, NDC 71288-0114-50, is a Meitheal Pharmaceuticals Inc. 1 g / 1 injection presentation packaged as 1 Vial, Single-Dose.
NDC search formats
- Canonical NDC 11: 71288-0114-50
- Digits-only NDC 11: 71288011450
- Possible 10-digit display format: 71288-114-50 (7128811450)
Helpful product links
- Search by brand name: Gemcitabine
- NDC 11: 71288-0114-50
- Product family NDC: 71288-0114
- VA classification code: AN900
- VA classification code description: ANTINEOPLASTIC,OTHER
- CMOP ID: G0143
- VUID: 4012914