NDC 41163-647

equaline ibuprofen

Ibuprofen

equaline ibuprofen is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Supervalu Inc. The primary component is Ibuprofen.

• Product ID: 41163-647_18f1f934-7b49-4632-9eb3-45206d5d51f6
• NDC: 41163-647
• Product Type: Human Otc Drug
• Proprietary Name: equaline ibuprofen
• Generic Name: Ibuprofen
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2004-08-17
• Marketing Category: ANDA / ANDA
• Application Number: ANDA072096
• Labeler Name: Supervalu Inc
• Substance Name: IBUPROFEN
• Active Ingredient Strength: 200 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 41163-647-71

1 BOTTLE in 1 CARTON (41163-647-71) > 50 TABLET, FILM COATED in 1 BOTTLE

• Marketing Start Date: 2004-08-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 41163-647-62 [41163064762]

equaline ibuprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA072096
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-08-17
• Marketing End Date: 2013-04-23

NDC 41163-647-76 [41163064776]

equaline ibuprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA072096
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-12-06

NDC 41163-647-72 [41163064772]

equaline ibuprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA072096
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-30

NDC 41163-647-71 [41163064771]

equaline ibuprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA072096
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-08-30

NDC 41163-647-78 [41163064778]

equaline ibuprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA072096
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-08-17

Drug Details

Active Ingredients

Ingredient	Strength
IBUPROFEN	200 mg/1

OpenFDA Data

• SPL SET ID: 9bf3546a-9f94-47b5-9b01-aed93e69d5aa
• Manufacturer:
  • Supervalu Inc
• UNII:
  • WK2XYI10QM
• RxNorm Concept Unique ID - RxCUI:
  • 310965
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
• NUI Code:
  • N0000000160
  • N0000175722
  • N0000175721

NDC Crossover Matching brand name "equaline ibuprofen" or generic name "Ibuprofen"

NDC	Brand Name	Generic Name
41163-521	equaline ibuprofen	equaline ibuprofen
41163-057	Equaline Ibuprofen	Equaline Ibuprofen
41163-255	equaline ibuprofen	equaline ibuprofen
41163-685	Equaline Ibuprofen	Equaline Ibuprofen
41163-647	equaline ibuprofen	equaline ibuprofen
41163-604	equaline ibuprofen	equaline ibuprofen
0113-1461	basic care childrens ibuprofen	Ibuprofen
0113-7619	basic care childrens ibuprofen	ibuprofen
0113-7660	basic care childrens ibuprofen	Ibuprofen
0113-7897	Basic Care childrens ibuprofen	Ibuprofen
0113-0788	Basic Care ibuprofen	Ibuprofen
0113-7131	basic care ibuprofen	Ibuprofen
0113-7517	basic care ibuprofen	Ibuprofen
0113-7604	Basic Care Ibuprofen	Ibuprofen
0121-0917	Childrens Ibuprofen	Ibuprofen
0121-0914	Childrens Ibuprofen Oral Suspension	Ibuprofen
0113-2461	Good Sense Childrens Ibuprofen	Ibuprofen
0113-0057	Good Sense ibuprofen	ibuprofen
0113-0074	Good Sense ibuprofen	Ibuprofen
0113-0166	good sense ibuprofen	Ibuprofen
0113-0298	good sense ibuprofen	Ibuprofen
0113-0461	Good Sense ibuprofen	Ibuprofen
0113-0517	Good Sense ibuprofen	Ibuprofen
0113-0604	good sense ibuprofen	Ibuprofen
0113-0647	good sense ibuprofen	Ibuprofen
0113-0660	Good Sense Ibuprofen	Ibuprofen
0113-0685	Good Sense Ibuprofen	Ibuprofen
0113-0897	good sense ibuprofen	Ibuprofen
0113-1212	Good Sense Ibuprofen	Ibuprofen
0113-4501	good sense ibuprofen	ibuprofen
0113-0040	Good Sense Infants Ibuprofen	Ibuprofen