Oxaliplatin 67184-0502

Product NDC

67184-0502

Manufacturer: Qilu Pharmaceutical Co., Ltd.
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: May 11, 2016
Listing Expires: December 31, 2026
Application: ANDA204616

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Active Ingredients

Ingredient	Strength
Oxaliplatin	100 mg/20mL

Drug Class

Platinum-based Drug [EPC]Platinum-based Drug [EPC]Platinum-containing Compounds [EXT]

Packaging Options(1)

67184-0502-01

1 VIAL, SINGLE-DOSE in 1 CARTON (67184-0502-1) / 20 mL in 1 VIAL, SINGLE-DOSE

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