NDC 11673-991

IBUPROFEN

Ibuprofen

IBUPROFEN is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Ibuprofen.

Product ID11673-991_9dea0327-d1d6-58f2-e053-2a95a90a023e
NDC11673-991
Product TypeHuman Otc Drug
Proprietary NameIBUPROFEN
Generic NameIbuprofen
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2020-02-04
Marketing CategoryANDA / ANDA
Application NumberANDA091239
Labeler NameTARGET CORPORATION
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 11673-991-01

100 TABLET, COATED in 1 BOTTLE (11673-991-01)
Marketing Start Date2020-02-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11673-991-01 [11673099101]

IBUPROFEN TABLET, COATED
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-02-04

NDC 11673-991-05 [11673099105]

IBUPROFEN TABLET, COATED
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-02-04

NDC 11673-991-20 [11673099120]

IBUPROFEN TABLET, COATED
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-02-04

NDC 11673-991-88 [11673099188]

IBUPROFEN TABLET, COATED
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-02-04

NDC 11673-991-26 [11673099126]

IBUPROFEN TABLET, COATED
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-02-04
Marketing End Date2020-02-06

NDC 11673-991-50 [11673099150]

IBUPROFEN TABLET, COATED
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-02-04

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

NDC Crossover Matching brand name "IBUPROFEN" or generic name "Ibuprofen"

NDCBrand NameGeneric Name
67877-120ibuprofenibuprofen
67877-119ibuprofenibuprofen
67877-295ibuprofenibuprofen
67877-121ibuprofenibuprofen
67877-294ibuprofenibuprofen
67877-296ibuprofenibuprofen
67877-321IbuprofenIbuprofen
67877-319IbuprofenIbuprofen
67877-320IbuprofenIbuprofen
68016-116IbuprofenIbuprofen
68016-633IbuprofenIbuprofen
68016-626IbuprofenIbuprofen
68016-634IbuprofenIbuprofen
68016-645IbuprofenIbuprofen
68016-295IbuprofenIbuprofen
68016-635IbuprofenIbuprofen
68071-3074IbuprofenIbuprofen
68071-3362IBUPROFENIBUPROFEN
68071-4129IbuprofenIbuprofen
68071-4009IBUPROFENIBUPROFEN
68071-3388IbuprofenIbuprofen
68071-4253IbuprofenIbuprofen
68071-4306IbuprofenIbuprofen
68071-4357IbuprofenIbuprofen
68071-4563IbuprofenIbuprofen
68071-4280IbuprofenIbuprofen
68071-4243IBUPROFENIBUPROFEN
68071-4820IbuprofenIbuprofen
68071-4305IbuprofenIbuprofen
68071-4459IBUPROFENIBUPROFEN
68084-703IbuprofenIbuprofen
68084-658IbuprofenIbuprofen
68084-772IbuprofenIbuprofen
68196-980IbuprofenIbuprofen
68196-981IbuprofenIbuprofen
68210-0200IBUPROFENIBUPROFEN
68196-199IbuprofenIbuprofen
68210-0009IBUPROFENIBUPROFEN
68196-745IbuprofenIbuprofen
68387-208IbuprofenIbuprofen
0472-2002IbuprofenIbuprofen
68387-210IbuprofenIbuprofen
68391-121IbuprofenIbuprofen
68391-199IbuprofenIbuprofen
0472-1270IbuprofenIbuprofen
68645-531IbuprofenIbuprofen
68645-563IbuprofenIbuprofen
68645-562IbuprofenIbuprofen
68645-561IbuprofenIbuprofen
0113-1461basic care childrens ibuprofenIbuprofen

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.