NDC 21695-039

diclofenac sodium

Diclofenac Sodium

diclofenac sodium is a Oral Tablet, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors Corp. The primary component is Diclofenac Sodium.

• Product ID: 21695-039_6b7fb6b7-2f58-4cb6-b48f-e9b4cf292365
• NDC: 21695-039
• Product Type: Human Prescription Drug
• Proprietary Name: diclofenac sodium
• Generic Name: Diclofenac Sodium
• Dosage Form: Tablet, Delayed Release
• Route of Administration: ORAL
• Marketing Start Date: 1996-03-26
• Marketing Category: ANDA / ANDA
• Application Number: ANDA074514
• Labeler Name: Rebel Distributors Corp
• Substance Name: DICLOFENAC SODIUM
• Active Ingredient Strength: 75 mg/1
• Pharm Classes: Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 21695-039-60

60 TABLET, DELAYED RELEASE in 1 BOTTLE (21695-039-60)

• Marketing Start Date: 1996-03-26
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 21695-039-60 [21695003960]

diclofenac sodium TABLET, DELAYED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA074514
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1996-03-26
• Inactivation Date: 2019-09-24

NDC 21695-039-30 [21695003930]

diclofenac sodium TABLET, DELAYED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA074514
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1996-03-26
• Inactivation Date: 2019-09-24

NDC 21695-039-20 [21695003920]

diclofenac sodium TABLET, DELAYED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA074514
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1996-03-26
• Inactivation Date: 2019-09-24

NDC 21695-039-90 [21695003990]

diclofenac sodium TABLET, DELAYED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA074514
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1996-03-26
• Inactivation Date: 2019-09-24

Drug Details

Active Ingredients

Ingredient	Strength
DICLOFENAC SODIUM	75 mg/1

OpenFDA Data

• SPL SET ID: 6b7fb6b7-2f58-4cb6-b48f-e9b4cf292365
• Manufacturer:
  • Rebel Distributors Corp
• UNII:
  • QTG126297Q
• RxNorm Concept Unique ID - RxCUI:
  • 855926
  • 855906

Pharmacological Class

• 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"

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