NDC 70020-1910

IXEMPRA

Ixabepilone

IXEMPRA is a Kit in the Human Prescription Drug category. It is labeled and distributed by R-pharm Us Operating, Llc. The primary component is .

• Product ID: 70020-1910_7c37fa0c-a704-31be-e053-2a91aa0a931f
• NDC: 70020-1910
• Product Type: Human Prescription Drug
• Proprietary Name: IXEMPRA
• Generic Name: Ixabepilone
• Dosage Form: Kit
• Marketing Start Date: 2007-10-16
• Marketing Category: NDA / NDA
• Application Number: NDA022065
• Labeler Name: R-Pharm US Operating, LLC
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 70020-1910-1

1 KIT in 1 PACKAGE, COMBINATION (70020-1910-1) * 15 mg in 1 VIAL, SINGLE-USE * 8 mL in 1 VIAL, SINGLE-USE

• Marketing Start Date: 2007-10-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70020-1910-1 [70020191001]

IXEMPRA KIT

• Marketing Category: NDA
• Application Number: NDA022065
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2007-10-16

Drug Details

OpenFDA Data

• SPL SET ID: 241f0b1e-8b95-470d-876f-bf1804daaf18
• Manufacturer:
  • R-Pharm US Operating, LLC
• RxNorm Concept Unique ID - RxCUI:
  • 1726278
  • 1726271
  • 1726274
  • 1726276
• UPC Code:
  • 0370020000008

NDC Crossover Matching brand name "IXEMPRA" or generic name "Ixabepilone"

NDC	Brand Name	Generic Name
70020-1910	IXEMPRA	ixabepilone
70020-1911	IXEMPRA	ixabepilone