NDC 55289-066

Chlorpropamide

Chlorpropamide

Chlorpropamide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Pd-rx Pharmaceuticals, Inc.. The primary component is Chlorpropamide.

• Product ID: 55289-066_7b97c681-4516-c544-e053-2991aa0a3d78
• NDC: 55289-066
• Product Type: Human Prescription Drug
• Proprietary Name: Chlorpropamide
• Generic Name: Chlorpropamide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1984-06-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA088549
• Labeler Name: PD-Rx Pharmaceuticals, Inc.
• Substance Name: CHLORPROPAMIDE
• Active Ingredient Strength: 250 mg/1
• Pharm Classes: Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 55289-066-90

90 TABLET in 1 BOTTLE, PLASTIC (55289-066-90)

• Marketing Start Date: 2009-02-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55289-066-90 [55289006690]

Chlorpropamide TABLET

• Marketing Category: ANDA
• Application Number: ANDA088549
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-02-25
• Marketing End Date: 2019-06-04

Drug Details

Active Ingredients

Ingredient	Strength
CHLORPROPAMIDE	250 mg/1

OpenFDA Data

• SPL SET ID: ae6af35a-b7b4-4520-ac40-8e4a6eb80bb1
• Manufacturer:
  • PD-Rx Pharmaceuticals, Inc.
• UNII:
  • WTM2C3IL2X
• RxNorm Concept Unique ID - RxCUI:
  • 197496
• UPC Code:
  • 0355289066903

Pharmacological Class

• Sulfonylurea [EPC]
• Sulfonylurea Compounds [CS]

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

NDC	Brand Name	Generic Name
0378-0197	Chlorpropamide	chlorpropamide
0378-0210	Chlorpropamide	chlorpropamide
55289-066	Chlorpropamide	chlorpropamide