NDC 63323-278

Vinblastine Sulfate

Vinblastine Sulfate

Vinblastine Sulfate is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Fresenius Kabi Usa, Llc. The primary component is Vinblastine Sulfate.

• Product ID: 63323-278_9b01b466-fbca-f255-e053-2995a90ac92d
• NDC: 63323-278
• Product Type: Human Prescription Drug
• Proprietary Name: Vinblastine Sulfate
• Generic Name: Vinblastine Sulfate
• Dosage Form: Injection
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2000-07-12
• Marketing Category: ANDA / ANDA
• Application Number: ANDA089515
• Labeler Name: Fresenius Kabi USA, LLC
• Substance Name: VINBLASTINE SULFATE
• Active Ingredient Strength: 1 mg/mL
• Pharm Classes: Vinca Alkaloid [EPC],Vinca Alkaloids [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 63323-278-10

1 VIAL, MULTI-DOSE in 1 BOX (63323-278-10) > 10 mL in 1 VIAL, MULTI-DOSE

• Marketing Start Date: 2000-07-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63323-278-10 [63323027810]

Vinblastine Sulfate INJECTION

• Marketing Category: ANDA
• Application Number: ANDA089515
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2000-07-12

Drug Details

Active Ingredients

Ingredient	Strength
VINBLASTINE SULFATE	1 mg/mL

OpenFDA Data

• SPL SET ID: f073b58e-56d6-4c8d-a2ce-b37719402d77
• Manufacturer:
  • Fresenius Kabi USA, LLC
• UNII:
  • N00W22YO2B
• RxNorm Concept Unique ID - RxCUI:
  • 239178

Pharmacological Class

• Vinca Alkaloid [EPC]
• Vinca Alkaloids [CS]