NDC 50844-352

Ibuprofen

Ibuprofen

Ibuprofen is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by L.n.k. International, Inc.. The primary component is Ibuprofen.

Product ID50844-352_32aab705-6886-443e-81ad-cfe0c72053ed
NDC50844-352
Product TypeHuman Otc Drug
Proprietary NameIbuprofen
Generic NameIbuprofen
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1999-03-01
Marketing CategoryANDA / ANDA
Application NumberANDA075139
Labeler NameL.N.K. International, Inc.
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 50844-352-02

1 BOTTLE, PLASTIC in 1 CARTON (50844-352-02) > 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing Start Date1999-03-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50844-352-16 [50844035216]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-03-01

NDC 50844-352-12 [50844035212]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-03-01

NDC 50844-352-02 [50844035202]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-03-01

NDC 50844-352-15 [50844035215]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-03-01

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.