Ibuprofen NDC 50844-291

Product information

Brand name (proprietary)

Ibuprofen

Generic name (nonproprietary)

ibuprofen

Active ingredients

Ibuprofen — 200 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

L.N.K. International, Inc.

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 075010

Marketing start

May 24, 1988

Listing expires

Dec 31, 2027

Other FDA classes

Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)

Identifiers

Product ID 50844-291_6de067d7-e53a-48a0-8cf4-bf7d41fa02e0SPL ID 6de067d7-e53a-48a0-8cf4-bf7d41fa02e0SPL set ID 57b39311-bc20-ace6-75a9-a07a9311b373RxCUI 310965UNII WK2XYI10QMUPC 0350844291165

Pharmacologic class

Nonsteroidal Anti-inflammatory Drug

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450844029101 followed by a unit qualifier and the quantity Copy

Package 50844-0291-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Other NDCs under ANDA 075010

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

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