NDC 71335-1238

Diclofenac Sodium

Diclofenac Sodium

Diclofenac Sodium is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Diclofenac Sodium.

Product ID71335-1238_5be76dd2-b3d9-44a0-8500-2b1a3cbc2101
NDC71335-1238
Product TypeHuman Prescription Drug
Proprietary NameDiclofenac Sodium
Generic NameDiclofenac Sodium
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2002-11-06
Marketing CategoryANDA / ANDA
Application NumberANDA076201
Labeler NameBryant Ranch Prepack
Substance NameDICLOFENAC SODIUM
Active Ingredient Strength100 mg/1
Pharm ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-1238-1

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1238-1)
Marketing Start Date2019-06-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1238-1 [71335123801]

Diclofenac Sodium TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076201
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-06-06

NDC 71335-1238-7 [71335123807]

Diclofenac Sodium TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076201
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-06-06

NDC 71335-1238-8 [71335123808]

Diclofenac Sodium TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076201
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-06-06

NDC 71335-1238-5 [71335123805]

Diclofenac Sodium TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076201
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-06-06

NDC 71335-1238-2 [71335123802]

Diclofenac Sodium TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076201
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-06-06

NDC 71335-1238-4 [71335123804]

Diclofenac Sodium TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076201
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-06-06

NDC 71335-1238-3 [71335123803]

Diclofenac Sodium TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076201
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-06-06

NDC 71335-1238-6 [71335123806]

Diclofenac Sodium TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076201
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-06-06

Drug Details

Active Ingredients

IngredientStrength
DICLOFENAC SODIUM100 mg/1

OpenFDA Data

SPL SET ID:e9ece848-3cd3-4a75-be88-d131775016a7
Manufacturer
UNII

Pharmacological Class

  • Cyclooxygenase Inhibitors [MoA]
  • Decreased Prostaglandin Production [PE]
  • Anti-Inflammatory Agents
  • Non-Steroidal [CS]
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • Cyclooxygenase Inhibitors [MoA]
  • Decreased Prostaglandin Production [PE]
  • Anti-Inflammatory Agents
  • Non-Steroidal [CS]
  • Nonsteroidal Anti-inflammatory Drug [EPC]

NDC Crossover Matching brand name "Diclofenac Sodium" or generic name "Diclofenac Sodium"

NDCBrand NameGeneric Name
0115-1483Diclofenac SodiumDiclofenac Sodium
0168-0803DICLOFENAC SODIUMdiclofenac sodium
0168-0844DICLOFENAC SODIUMdiclofenac sodium
0228-2550Diclofenac SodiumDiclofenac Sodium
0228-2551Diclofenac SodiumDiclofenac Sodium
0363-1210Diclofenac sodiumDiclofenac sodium
0363-1871diclofenac sodiumdiclofenac sodium
0378-0355Diclofenac SodiumDiclofenac Sodium
0378-6280Diclofenac Sodiumdiclofenac sodium
0378-6281Diclofenac Sodiumdiclofenac sodium
67544-899Diclofenac SodiumDiclofenac Sodium
68001-200Diclofenac SodiumDiclofenac Sodium
68001-201Diclofenac SodiumDiclofenac Sodium
68001-202Diclofenac SodiumDiclofenac Sodium
68001-279Diclofenac SodiumDiclofenac Sodium
68001-280Diclofenac SodiumDiclofenac Sodium
68001-281Diclofenac SodiumDiclofenac Sodium
68071-2045Diclofenac SodiumDiclofenac Sodium
68071-3159Diclofenac sodiumDiclofenac sodium
68071-3325Diclofenac SodiumDiclofenac Sodium
68071-3132Diclofenac SodiumDiclofenac Sodium
68071-4158Diclofenac SodiumDiclofenac Sodium
68071-4382Diclofenac SodiumDiclofenac Sodium
68071-4246Diclofenac sodiumDiclofenac sodium
68084-333Diclofenac SodiumDiclofenac Sodium
68151-0849Diclofenac SodiumDiclofenac Sodium
68151-2481Diclofenac SodiumDiclofenac Sodium
68180-538Diclofenac SodiumDiclofenac Sodium
0472-1783Diclofenac SodiumDiclofenac Sodium
68387-260Diclofenac SodiumDiclofenac Sodium
68382-999Diclofenac sodiumDiclofenac sodium
68462-355DICLOFENAC SODIUMDICLOFENAC SODIUM
68682-103Diclofenac SodiumDiclofenac Sodium
68788-7270Diclofenac SodiumDiclofenac Sodium
68788-6368Diclofenac SodiumDiclofenac Sodium
68788-6388Diclofenac SodiumDiclofenac Sodium
68788-6831Diclofenac sodiumDiclofenac sodium
68788-7225Diclofenac sodiumDiclofenac sodium
68788-7097Diclofenac SodiumDiclofenac Sodium
68788-6952Diclofenac SodiumDiclofenac Sodium
68788-9231Diclofenac SodiumDiclofenac Sodium
68788-9389Diclofenac SodiumDiclofenac Sodium
68788-9523Diclofenac SodiumDiclofenac Sodium
68788-9175Diclofenac SodiumDiclofenac Sodium
68788-9185Diclofenac SodiumDiclofenac Sodium
68788-9435DICLOFENAC SODIUMDICLOFENAC SODIUM
69097-524Diclofenac SodiumDiclofenac Sodium
0527-2170Diclofenac SodiumDiclofenac Sodium
69621-300Diclofenac SodiumDiclofenac Sodium
69837-399DICLOFENAC SODIUMDICLOFENAC SODIUM
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