NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7653Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7653Add 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
50090-7653-0500907653001 BOTTLE, PLASTIC in 1 CARTON (50090-7653-0) / 120 mL in 1 BOTTLE, PLASTICMarketed from Sep 9, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 100 mg/5mL
Dosage form
Suspension
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211666
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 50090-7653_65d7cba1-ee25-42e5-908f-a0e1e3416914SPL ID 65d7cba1-ee25-42e5-908f-a0e1e3416914SPL set ID 7d4ba8be-df59-4a21-8850-8a59bf72b604RxCUI 197803UNII WK2XYI10QM

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

N450090765300 followed by a unit qualifier and the quantity

Package 50090-7653-00. 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 .

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211666

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

FDA NDC Directory listings under ANDA 211666
ProductStrengthForm · routeLabelerProduct NDC
ibuprofenIbuprofen 100 mg/5mLSuspensionOralSun Pharmaceutical Industries, Inc.51672-5321

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