NDC 16729-251 – bendamustine hydrochloride
Bendamustine Hydrochloride 100 mg/20mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC16729-251
Product details
- Brand name
- bendamustine hydrochloride
- Generic name
- bendamustine hydrochloride
- Labeler
- Accord Healthcare, Inc.
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA205574
- Marketed since
- December 7, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Alkylating Drug
Active ingredients
- Bendamustine Hydrochloride 100 mg/20mL
Uses, dosage, side effects and warnings for Bendamustine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16729-251-05 | 1 VIAL, SINGLE-DOSE in 1 CARTON (16729-251-05) / 20 mL in 1 VIAL, SINGLE-DOSE | Dec 7, 2022 |
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