Ibuprofen 71921-0180-50

Package NDC

71921-0180-50

Product NDC: 71921-0180

Manufacturer: Florida Pharmaceutical Products, Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 21, 2021
Listing Expires: December 31, 2026
Application: ANDA071268

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Active Ingredients

Ingredient	Strength
Ibuprofen	400 mg/1

Drug Class

Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]

Selected Package

71921-0180-50Selected

500 TABLET, FILM COATED in 1 BOTTLE (71921-180-50)

Other packages for this product(1)

71921-0180-01

100 TABLET, FILM COATED in 1 BOTTLE (71921-180-01)

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