NDC 0722-7121

Chenodiol

Chenodiol

Chenodiol is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Nexgen Pharma, Inc.. The primary component is Chenodiol.

• Product ID: 0722-7121_9aca5e67-d2c3-4e21-a584-4d90cfc70bd4
• NDC: 0722-7121
• Product Type: Human Prescription Drug
• Proprietary Name: Chenodiol
• Generic Name: Chenodiol
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2009-10-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA091019
• Labeler Name: Nexgen Pharma, Inc.
• Substance Name: CHENODIOL
• Active Ingredient Strength: 250 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0722-7121-01

1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0722-7121-01)

• Marketing Start Date: 2009-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0722-7121-01 [00722712101]

Chenodiol TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA091019
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-10-22

Drug Details

Active Ingredients

Ingredient	Strength
CHENODIOL	250 mg/1

OpenFDA Data

• SPL SET ID: bbb86251-9423-40e6-9117-9511ab5fbf63
• Manufacturer:
  • Nexgen Pharma, Inc.
• UNII:
  • 0GEI24LG0J
• RxNorm Concept Unique ID - RxCUI:
  • 618469

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

NDC	Brand Name	Generic Name
0722-7121	Chenodiol	Chenodiol
79739-7121	Chenodiol	Chenodiol
45043-876	Chenodal	Chenodiol
68974-876	Chenodal	Chenodiol