NDC 0143-9270

Floxuridine

Floxuridine

Floxuridine is a Intra-arterial Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by West-ward Pharmaceuticals Corp. The primary component is Floxuridine.

• Product ID: 0143-9270_2b1e7da5-63ad-497c-b41d-b1b1275de42d
• NDC: 0143-9270
• Product Type: Human Prescription Drug
• Proprietary Name: Floxuridine
• Generic Name: Floxuridine
• Dosage Form: Injection, Powder, Lyophilized, For Solution
• Route of Administration: INTRA-ARTERIAL
• Marketing Start Date: 2018-02-15
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075387
• Labeler Name: West-Ward Pharmaceuticals Corp
• Substance Name: FLOXURIDINE
• Active Ingredient Strength: 100 mg/mL
• Pharm Classes: Antimetabolite [EPC],Deoxyuridine [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0143-9270-01

1 VIAL in 1 BOX, UNIT-DOSE (0143-9270-01) > 5 mL in 1 VIAL

• Marketing Start Date: 2018-02-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0143-9270-01 [00143927001]

Floxuridine INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA075387
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-02-15

Drug Details

Active Ingredients

Ingredient	Strength
FLOXURIDINE	100 mg/mL

OpenFDA Data

• SPL SET ID: e3c2e3e7-bc83-465d-b615-3ad56580b3a7
• Manufacturer:
  • West-Ward Pharmaceuticals Corp
• UNII:
  • 039LU44I5M
• RxNorm Concept Unique ID - RxCUI:
  • 310351

Pharmacological Class

• Antimetabolite [EPC]
• Deoxyuridine [CS]

NDC Crossover Matching brand name "Floxuridine" or generic name "Floxuridine"

NDC	Brand Name	Generic Name
0143-9270	Floxuridine	Floxuridine
63323-145	Floxuridine	FLOXURIDINE
81643-9270	Floxuridine	Floxuridine