NDC 21695-065

Ibuprofen (NSAID) Pain Releiver/ Fever Reducer

Ibuprofen (nsaid)

Ibuprofen (NSAID) Pain Releiver/ Fever Reducer is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rebel Distributors Corp. The primary component is Ibuprofen.

• Product ID: 21695-065_7b4858fc-fea6-4e4c-886e-a2febe1ed2c3
• NDC: 21695-065
• Product Type: Human Otc Drug
• Proprietary Name: Ibuprofen (NSAID) Pain Releiver/ Fever Reducer
• Generic Name: Ibuprofen (nsaid)
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2009-12-16
• Marketing Category: ANDA / ANDA
• Application Number: ANDA071333
• Labeler Name: Rebel Distributors Corp
• Substance Name: IBUPROFEN
• Active Ingredient Strength: 200 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 21695-065-60

60 TABLET in 1 BOTTLE (21695-065-60)

• Marketing Start Date: 2009-12-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 21695-065-28 [21695006528]

Ibuprofen (NSAID) Pain Releiver/ Fever Reducer TABLET

• Marketing Category: ANDA
• Application Number: ANDA071333
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-16
• Inactivation Date: 2019-09-24

NDC 21695-065-14 [21695006514]

Ibuprofen (NSAID) Pain Releiver/ Fever Reducer TABLET

• Marketing Category: ANDA
• Application Number: ANDA071333
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-16
• Inactivation Date: 2019-09-24

NDC 21695-065-60 [21695006560]

Ibuprofen (NSAID) Pain Releiver/ Fever Reducer TABLET

• Marketing Category: ANDA
• Application Number: ANDA071333
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-16
• Inactivation Date: 2019-09-24

NDC 21695-065-30 [21695006530]

Ibuprofen (NSAID) Pain Releiver/ Fever Reducer TABLET

• Marketing Category: ANDA
• Application Number: ANDA071333
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-16
• Inactivation Date: 2019-09-24

NDC 21695-065-50 [21695006550]

Ibuprofen (NSAID) Pain Releiver/ Fever Reducer TABLET

• Marketing Category: ANDA
• Application Number: ANDA071333
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-16
• Inactivation Date: 2019-09-24

NDC 21695-065-06 [21695006506]

Ibuprofen (NSAID) Pain Releiver/ Fever Reducer TABLET

• Marketing Category: ANDA
• Application Number: ANDA071333
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-12-16
• Inactivation Date: 2019-09-24

NDC 21695-065-90 [21695006590]

Ibuprofen (NSAID) Pain Releiver/ Fever Reducer TABLET

• Marketing Category: ANDA
• Application Number: ANDA071333
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-16
• Inactivation Date: 2019-09-24

Drug Details

Active Ingredients

Ingredient	Strength
IBUPROFEN	200 mg/1

OpenFDA Data

• SPL SET ID: 7b4858fc-fea6-4e4c-886e-a2febe1ed2c3
• Manufacturer:
  • Rebel Distributors Corp
• 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 "Ibuprofen (NSAID) Pain Releiver/ Fever Reducer" or generic name "Ibuprofen (nsaid)"

NDC	Brand Name	Generic Name
53746-142	Ibuprofen (NSAID) Pain Releiver/ Fever Reducer	Ibuprofen (NSAID) Pain Releiver/ Fever Reducer
53746-144	Ibuprofen (NSAID) Pain Releiver/ Fever Reducer	Ibuprofen (NSAID) Pain Releiver/ Fever Reducer
21695-065	Ibuprofen (NSAID)	Ibuprofen (NSAID)