NDC codes

FDA NDC Directory
Product NDC (as listed)69367-448Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69367-0448Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
69367-448-0169367044801100 TABLET, FILM COATED in 1 BOTTLE (69367-448-01)Marketed from Mar 9, 2026
69367-448-0569367044805500 TABLET, FILM COATED in 1 BOTTLE (69367-448-05)Marketed from Mar 9, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Ibuprofen
Generic name (nonproprietary)
ibuprofen
Active ingredients
Ibuprofen — 600 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Westminster Pharmaceuticals, LLCNDC labeler code 69367
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215318
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 69367-448_a4e24f05-7843-49ee-be1a-28c1bef70523SPL ID a4e24f05-7843-49ee-be1a-28c1bef70523SPL set ID 6f7e255f-48c9-4366-8725-7f8cbe1bb75aRxCUI 197805, 197806, 197807UNII WK2XYI10QMUPC 0369367447010

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

N469367044801 followed by a unit qualifier and the quantity

Package 69367-0448-01. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of ibuprofen tablets and other treatment options before deciding to use ibuprofen. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals [see WARNINGS ]. Ibuprofen tablets are indicated for relief of the signs and symptoms of rheumatoid arthritis and osteoarthritis. Ibuprofen tablets are indicated for relief of mild to moderate pain. Ibuprofen tablets are also indicated for the treatment of primary dysmenorrhea. Controlled clinical trials to establish the safety and effectiveness of ibuprofen tablets in children have not been conducted.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69367-448

What is NDC 69367-448?
69367-448 is the product NDC for Ibuprofen, Ibuprofen 600 mg/1 tablet, film coated, listed with the FDA by Westminster Pharmaceuticals, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ibuprofen.
What is the active ingredient?
Ibuprofen.
Who is the labeler?
Westminster Pharmaceuticals, LLC, NDC labeler code 69367. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ibuprofen?
663 other product NDCs are listed under this name. See all Ibuprofen NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Ibuprofen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73967877-0739-0167877-0739-0567877-0739-30+4 more
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73767877-0737-0167877-0737-0567877-0737-33+1 more
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-73867877-0738-0167877-0738-0567877-0738-30+3 more
IbuprofenIbuprofen 200 mg/1Capsule, Liquid filledOralGOODSENSE50804-18550804-0185-0150804-0185-02
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralShield Pharmaceuticals Corp83059-018083059-0180-04
IbuprofenIbuprofen 200 mg/1Capsule, Liquid filledOralGobrands, Inc. (Goodnow)82501-101082501-1010-00
IbuprofenIbuprofen 600 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-474170518-4741-0070518-4741-02
IbuprofenIbuprofen 200 mg/1Tablet, CoatedOralP & L Development, LLC59726-00359726-0003-50
IbuprofenIbuprofen 200 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-14372288-0143-7872288-0143-90
IbuprofenIbuprofen 200 mg/1TabletOralNUVICARE LLC84324-03984324-0039-01

All 664 Ibuprofen NDCs

Other NDCs under ANDA 215318

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

FDA NDC Directory listings under ANDA 215318
ProductStrengthForm · routeLabelerProduct NDC
IbuprofenIbuprofen 400 mg/1Tablet, Film coatedOralWestminster Pharmaceuticals, LLC69367-447
IbuprofenIbuprofen 800 mg/1Tablet, Film coatedOralWestminster Pharmaceuticals, LLC69367-449

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