NDC 67184-0502 – Oxaliplatin
Oxaliplatin 100 mg/20mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC67184-0502
Product details
- Brand name
- Oxaliplatin
- Generic name
- Oxaliplatin
- Labeler
- Qilu Pharmaceutical Co., Ltd.
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA204616
- Marketed since
- May 11, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Platinum-based Drug
Active ingredients
- Oxaliplatin 100 mg/20mL
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 67184-0502-1 | 1 VIAL, SINGLE-DOSE in 1 CARTON (67184-0502-1) / 20 mL in 1 VIAL, SINGLE-DOSE | May 11, 2016 |
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