NDC 80425-0089

Motrin

Ibuprofen 800mg

Motrin is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Advanced Rx Pharmacy Of Tennessee, Llc. The primary component is Ibuprofen.

Product ID80425-0089_b4cd0cf5-db6d-7b49-e053-2a95a90a59af
NDC80425-0089
Product TypeHuman Prescription Drug
Proprietary NameMotrin
Generic NameIbuprofen 800mg
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2015-12-30
Marketing CategoryANDA / ANDA
Application NumberANDA090796
Labeler NameAdvanced Rx Pharmacy of Tennessee, LLC
Substance NameIBUPROFEN
Active Ingredient Strength800 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 80425-0089-4

60 TABLET, FILM COATED in 1 BOTTLE (80425-0089-4)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Motrin" or generic name "Ibuprofen 800mg"

NDCBrand NameGeneric Name
50580-198MotrinIbuprofen
50580-563MotrinIbuprofen and Diphenhydramine Citrate
80425-0046MotrinIbuprofen 800mg
80425-0047MotrinIbuprofen 800mg
80425-0089MotrinIbuprofen 800mg
80425-0154MotrinIbuprofen 600mg

Trademark Results [Motrin]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MOTRIN
MOTRIN
97348734 not registered Live/Pending
Johnson & Johnson
2022-04-06
MOTRIN
MOTRIN
97180305 not registered Live/Pending
Johnson & Johnson
2021-12-20
MOTRIN
MOTRIN
97180295 not registered Live/Pending
Johnson & Johnson
2021-12-20
MOTRIN
MOTRIN
97180167 not registered Live/Pending
Johnson & Johnson
2021-12-20
MOTRIN
MOTRIN
72363500 0904181 Live/Registered
UPJOHN COMPANY, THE
1970-06-24

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