What is NDC 50090-7789?

50090-7789 is the product NDC for Ibuprofen, Ibuprofen 400 mg/1 tablet, film coated, listed with the FDA by A-S Medication Solutions. It has 4 package NDCs, shown above in 10- and 11-digit form.

A-S Medication Solutions, NDC labeler code 50090. 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?

674 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ibuprofen NDC 50090-7789 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-7789Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-7789Add 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 NDC	11-digit (billing)	Package
50090-7789-0	5009077890050090778900	16 TABLET, FILM COATED in 1 BOTTLE (50090-7789-0)Marketed from Nov 24, 2025
50090-7789-1	5009077890150090778901	30 TABLET, FILM COATED in 1 BOTTLE (50090-7789-1)Marketed from Nov 24, 2025
50090-7789-3	5009077890350090778903	100 TABLET, FILM COATED in 1 BOTTLE (50090-7789-3)Marketed from Nov 24, 2025
50090-7789-4	5009077890450090778904	20 TABLET, FILM COATED in 1 BOTTLE (50090-7789-4)Marketed from Nov 24, 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 — 400 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: A-S Medication SolutionsNDC labeler code 50090
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202413
Marketing start: May 23, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 50090-7789_621a94e3-872b-4a93-9153-59b23ee88d83SPL ID 621a94e3-872b-4a93-9153-59b23ee88d83SPL set ID 47711610-6577-4805-a2ce-cf9b7cbfa812RxCUI 197805UNII WK2XYI10QM
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

N450090778900 followed by a unit qualifier and the quantity

Package 50090-7789-00. 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 Nov 26, 2025. 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 50090-7789

What is NDC 50090-7789?: 50090-7789 is the product NDC for Ibuprofen, Ibuprofen 400 mg/1 tablet, film coated, listed with the FDA by A-S Medication Solutions. It has 4 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?: A-S Medication Solutions, NDC labeler code 50090. 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?: 674 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4784	70518-4784-0070518-4784-01
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4786	70518-4786-00
Ibuprofen	Ibuprofen 200 mg/1	TabletOral	Famora Inc	87509-0004	87509-0004-05
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-724	82461-0724-90
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-725	82461-0725-90
Ibuprofen	Ibuprofen 200 mg/1	TabletOral	Aurohealth LLC	58602-913	58602-0913-1758602-0913-40
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-737	67877-0737-0167877-0737-0567877-0737-33+1 more
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-738	67877-0738-0167877-0738-0567877-0738-30+3 more
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-739	67877-0739-0167877-0739-0567877-0739-30+4 more
Ibuprofen	Ibuprofen 200 mg/1	Capsule, Liquid filledOral	GOODSENSE	50804-185	50804-0185-0150804-0185-02

All 675 Ibuprofen NDCs

Other NDCs under ANDA 202413

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

FDA NDC Directory listings under ANDA 202413
Product	Strength	Form · route	Labeler	Product NDC
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	AiPing Pharmaceutical, Inc.	11788-008
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	AiPing Pharmaceutical, Inc.	11788-009
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	AiPing Pharmaceutical, Inc.	11788-010
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7281
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7282
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7283
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7286
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7288
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7320
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7321
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7788
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7905
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-8122
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-8124
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-8137
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-8138
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-8141
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-8142
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	ST. MARY'S MEDICAL PARK PHARMACY	60760-844
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	Chartwell RX, LLC	62135-400

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