NDC 0703-3125

Romidepsin

Romidepsin

Romidepsin is a Kit in the Human Prescription Drug category. It is labeled and distributed by Teva Parenteral Medicines, Inc.. The primary component is .

• Product ID: 0703-3125_109365f3-dfbd-4563-ad04-1df44476405a
• NDC: 0703-3125
• Product Type: Human Prescription Drug
• Proprietary Name: Romidepsin
• Generic Name: Romidepsin
• Dosage Form: Kit
• Marketing Start Date: 2018-08-01
• Marketing Category: NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
• Application Number: NDA022393
• Labeler Name: Teva Parenteral Medicines, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0703-3125-08

1 KIT in 1 CARTON (0703-3125-08) * 2 mL in 1 VIAL, GLASS * 2 mL in 1 VIAL, GLASS

• Marketing Start Date: 2018-08-01
• Marketing End Date: 2021-10-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0703-3125-08 [00703312508]

Romidepsin KIT

• Marketing Category: NDA AUTHORIZED GENERIC
• Application Number: NDA022393
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-08-01
• Marketing End Date: 2021-10-31

Drug Details

OpenFDA Data

• SPL SET ID: d7a653af-cfdb-457a-84cb-f04f11f61ba9
• Manufacturer:
  • Teva Parenteral Medicines, Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 877513

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

NDC	Brand Name	Generic Name
0069-0983	Romidepsin	romidepsin
0703-3071	Romidepsin	Romidepsin
0703-3125	Romidepsin	romidepsin
0703-4004	Romidepsin	Romidepsin
63323-926	Romidepsin	Romidepsin
59572-984	ISTODAX	romidepsin