NDC 70199-013

TRIGLIDE

Fenofibrate

TRIGLIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Casper Pharma Llc. The primary component is Fenofibrate.

• Product ID: 70199-013_59c22681-7513-49c9-a420-b711f6f14976
• NDC: 70199-013
• Product Type: Human Prescription Drug
• Proprietary Name: TRIGLIDE
• Generic Name: Fenofibrate
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2017-02-01
• Marketing Category: NDA / NDA
• Application Number: NDA021350
• Labeler Name: Casper Pharma LLC
• Substance Name: FENOFIBRATE
• Active Ingredient Strength: 160 mg/1
• Pharm Classes: Peroxisome Proliferator Receptor alpha Agonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 70199-013-30

1 BOTTLE in 1 CARTON (70199-013-30) > 30 TABLET in 1 BOTTLE

• Marketing Start Date: 2017-02-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70199-013-30 [70199001330]

TRIGLIDE TABLET

• Marketing Category: NDA
• Application Number: NDA021350
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-02-01

Drug Details

Active Ingredients

Ingredient	Strength
FENOFIBRATE	160 mg/1

OpenFDA Data

• SPL SET ID: de93ca37-e911-4520-b6b4-437aba03ae70
• Manufacturer:
  • Casper Pharma LLC
• UNII:
  • U202363UOS
• RxNorm Concept Unique ID - RxCUI:
  • 349287
  • 583096

Pharmacological Class

• Peroxisome Proliferator Receptor alpha Agonist [EPC]

NDC Crossover Matching brand name "TRIGLIDE" or generic name "Fenofibrate"

NDC	Brand Name	Generic Name
70199-013	TRIGLIDE	TRIGLIDE
59630-485	TRIGLIDE	TRIGLIDE
0093-7755	Fenofibrate	Fenofibrate
0093-7756	Fenofibrate	Fenofibrate
0115-0511	Fenofibrate	FENOFIBRATE
0115-0522	Fenofibrate	FENOFIBRATE
0115-0533	Fenofibrate	FENOFIBRATE
0115-1522	Fenofibrate	Fenofibrate
0115-1523	Fenofibrate	Fenofibrate
0115-5511	FENOFIBRATE	FENOFIBRATE
0115-5522	FENOFIBRATE	FENOFIBRATE
0074-3173	Tricor	Fenofibrate
0074-3189	Tricor	Fenofibrate