NDC 50192-113

CAMBIA

Diclofenac Potassium

CAMBIA is a Oral Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Nautilus Neurosciences, Inc.. The primary component is Diclofenac Potassium.

• Product ID: 50192-113_3a38ddb1-2e6b-406e-8992-a1c9cbd9acd0
• NDC: 50192-113
• Product Type: Human Prescription Drug
• Proprietary Name: CAMBIA
• Generic Name: Diclofenac Potassium
• Dosage Form: Powder, For Solution
• Route of Administration: ORAL
• Marketing Start Date: 2010-04-20
• Marketing Category: NDA / NDA
• Application Number: NDA022165
• Labeler Name: Nautilus Neurosciences, Inc.
• Substance Name: DICLOFENAC POTASSIUM
• Active Ingredient Strength: 1 mg/mg
• 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 50192-113-01

50 mg in 1 PACKET (50192-113-01)

• Marketing Start Date: 2010-04-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50192-113-03 [50192011303]

CAMBIA POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA022165
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-04-20
• Marketing End Date: 2012-04-02

NDC 50192-113-01 [50192011301]

CAMBIA POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA022165
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-04-20
• Inactivation Date: 2019-11-13

NDC 50192-113-09 [50192011309]

CAMBIA POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA022165
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-04-20
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
DICLOFENAC POTASSIUM	1 mg/mg

OpenFDA Data

• SPL SET ID: d7335594-50c9-4ae2-a3e3-b9a375187b62
• Manufacturer:
  • Nautilus Neurosciences, Inc.
• UNII:
  • L4D5UA6CB4
• RxNorm Concept Unique ID - RxCUI:
  • 859066
  • 859063

Pharmacological Class

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

Medicade Reported Pricing

50192011309 CAMBIA 50 MG POWDER PACKET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "CAMBIA" or generic name "Diclofenac Potassium"

NDC	Brand Name	Generic Name
13913-011	Cambia	diclofenac potassium
13913-012	Cambia	diclofenac potassium
50192-113	CAMBIA	Diclofenac Potassium
0093-0948	Diclofenac Potassium	Diclofenac Potassium
0378-2474	Diclofenac Potassium	diclofenac potassium
0480-9435	Diclofenac potassium	diclofenac potassium
0781-5017	Diclofenac Potassium	Diclofenac Potassium
12634-827	DICLOFENAC POTASSIUM	DICLOFENAC POTASSIUM
21695-838	Diclofenac Potassium	Diclofenac Potassium
23155-840	diclofenac potassium	diclofenac potassium
31722-046	Diclofenac potassium	Diclofenac potassium
33261-038	Diclofenac Potassium	Diclofenac Potassium
35356-713	Diclofenac Potassium	Diclofenac Potassium
43063-848	Diclofenac Potassium	Diclofenac Potassium
49884-905	Diclofenac Potassium	Diclofenac Potassium
50090-0646	Diclofenac Potassium	Diclofenac Potassium
50090-0647	Diclofenac Potassium	Diclofenac Potassium
50090-1535	Diclofenac Potassium	diclofenac potassium
50090-5893	Diclofenac Potassium	diclofenac potassium
15370-180	LOFENA	DICLOFENAC POTASSIUM
13913-008	ZIPSOR	diclofenac potassium