Bendamustine hydrochloride 100 mg / 20mL Injection 20 mL
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 68001-0572-41 |
|---|---|
| Product NDC | 68001-0572 |
| Generic Drug Name | bendamustine hydrochloride |
| Brand Name | bendamustine hydrochloride |
| Manufacturer | BluePoint Laboratories |
| Strength | 100 mg / 20mL |
| Dosage Form | Injection |
| Drug Type | Intravenous |
| Package Quantity | 1 Vial, Single-Dose |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-572-41) / 20 mL in 1 VIAL, SINGLE-DOSE |
| Active Ingredients | Bendamustine Hydrochloride |
| Marketing Category | ANDA |
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NDC snapshot
bendamustine hydrochloride 100 mg / 20mL Injection is tracked under NDC 68001-0572-41 and rolls up into product family 68001-0572. 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: BluePoint Laboratories.
- Dosage form: Injection.
- Family size: 1 indexed presentation.
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Official references
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Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 5 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
Bendamustine hydrochloride 100 mg / 20mL Injection 20 mL, NDC 68001-0572-41, is a BluePoint Laboratories 100 mg / 20mL injection presentation packaged as 1 Vial, Single-Dose.
NDC search formats
- Canonical NDC 11: 68001-0572-41
- Digits-only NDC 11: 68001057241
- Possible 10-digit display format: 68001-572-41 (6800157241)
Helpful product links
- Search by brand name: bendamustine hydrochloride
- NDC 11: 68001-0572-41
- Product family NDC: 68001-0572
- VA classification code: AN100
- VA classification code description: ANTINEOPLASTICS,ALKYLATING AGENTS
- CMOP ID: B0604
- VUID: 4027300