50090-5223 : Ibuprofen 200 mg Oral Tablet, Film Coated

NDC:	50090-5223
Labeler:	A-s Medication Solutions
Product Type:	Human OTC Drug
Drug Name:	Ibuprofen
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA072096
Rev. Date:	Sep 20, 2018

NDC Package Codes:

50090-5223-0: 50 TABLET, FILM COATED IN 1 BOTTLE (50090‑5223‑0)
50090-5223-2: 20 TABLET, FILM COATED IN 1 BOTTLE (50090‑5223‑2)
50090-5223-3: 24 TABLET, FILM COATED IN 1 BOTTLE (50090‑5223‑3)
50090-5223-4: 40 TABLET, FILM COATED IN 1 BOTTLE (50090‑5223‑4)
50090-5223-5: 30 TABLET, FILM COATED IN 1 BOTTLE (50090‑5223‑5)
50090-5223-6: 28 TABLET, FILM COATED IN 1 BOTTLE (50090‑5223‑6)
50090-5223-7: 60 TABLET, FILM COATED IN 1 BOTTLE (50090‑5223‑7)
50090-5223-8: 100 TABLET, FILM COATED IN 1 BOTTLE (50090‑5223‑8)

Active Ingredients:

Ibuprofen

Dosage Strength:

200 mg

Pharmaceutical Classes:

Anti-Inflammatory Agents
Non-Steroidal [CS]
Cyclooxygenase Inhibitors [MoA]
Nonsteroidal Anti-inflammatory Drug [EPC]

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.