NDC 68788-7341

Flurbiprofen

Flurbiprofen

Flurbiprofen is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Flurbiprofen.

• Product ID: 68788-7341_0b0640ee-35f8-4f40-9a2c-9feecda3df25
• NDC: 68788-7341
• Product Type: Human Prescription Drug
• Proprietary Name: Flurbiprofen
• Generic Name: Flurbiprofen
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2019-03-08
• Marketing Category: ANDA / ANDA
• Application Number: ANDA074431
• Labeler Name: Preferred Pharmaceuticals Inc.
• Substance Name: FLURBIPROFEN
• Active Ingredient Strength: 100 mg/1
• Pharm Classes: Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 68788-7341-1

100 TABLET, FILM COATED in 1 BOTTLE (68788-7341-1)

• Marketing Start Date: 2019-03-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68788-7341-1 [68788734101]

Flurbiprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA074431
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-03-08

NDC 68788-7341-3 [68788734103]

Flurbiprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA074431
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-03-08

NDC 68788-7341-9 [68788734109]

Flurbiprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA074431
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-03-08

NDC 68788-7341-6 [68788734106]

Flurbiprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA074431
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-03-08

Drug Details

Active Ingredients

Ingredient	Strength
FLURBIPROFEN	100 mg/1

OpenFDA Data

• SPL SET ID: a0e9620d-0951-44d7-af6c-9b642051bd74
• Manufacturer:
  • Preferred Pharmaceuticals Inc.
• UNII:
  • 5GRO578KLP
• RxNorm Concept Unique ID - RxCUI:
  • 197724
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
• NUI Code:
  • N0000000160
  • N0000175722
  • N0000175721

Pharmacological Class

• Cyclooxygenase Inhibitors [MoA]
• Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
• Nonsteroidal Anti-inflammatory Drug [EPC]

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

NDC	Brand Name	Generic Name
0093-0711	Flurbiprofen	Flurbiprofen
0378-0076	Flurbiprofen	flurbiprofen
0378-0093	Flurbiprofen	flurbiprofen
43063-992	Flurbiprofen	Flurbiprofen
45865-918	Flurbiprofen	Flurbiprofen
49999-311	Flurbiprofen	Flurbiprofen
50090-0509	Flurbiprofen	Flurbiprofen
55289-561	Flurbiprofen	flurbiprofen
63629-8338	Flurbiprofen	Flurbiprofen
63629-8808	Flurbiprofen	Flurbiprofen
68071-2480	Flurbiprofen	Flurbiprofen
68071-4436	Flurbiprofen	Flurbiprofen
68788-7341	Flurbiprofen	Flurbiprofen
69642-1300	Antiphlamine Pain Relieving	Flurbiprofen