Drugplain

NDC 61919-463-15

IBUPROFEN 800 mg/1

IBUOROFEN · TABLET, FILM COATED

No Recall History

IBUPROFEN is a tablet, film coated containing ibuorofen at a strength of 800 mg/1. Manufactured by Direct_Rx.

Key Facts

Brand Name
IBUPROFEN
Generic Name
IBUOROFEN
NDC Code (Package)
61919-463-15
NDC Code (Product)
61919-463
Manufacturer
Direct_Rx
Strength
800 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA091625
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing Start
08/22/2019

Recall History

No Recall History

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Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.