NDC 50844-292

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 ID50844-292_1538c30f-65db-4206-aa0c-e50afb531f7d
NDC50844-292
Product TypeHuman Otc Drug
Proprietary NameIbuprofen
Generic NameIbuprofen
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1988-05-24
Marketing CategoryANDA / ANDA
Application NumberANDA075010
Labeler NameL.N.K. International, Inc.
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 50844-292-00

250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-292-00)
Marketing Start Date1988-05-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50844-292-02 [50844029202]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 50844-292-11 [50844029211]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 50844-292-12 [50844029212]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 50844-292-13 [50844029213]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 50844-292-00 [50844029200]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 50844-292-16 [50844029216]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 50844-292-01 [50844029201]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 50844-292-15 [50844029215]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 50844-292-14 [50844029214]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 50844-292-08 [50844029208]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

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
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