What is NDC 59651-908?

59651-908 is the product NDC for Ibuprofen and famotidine, Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 tablet, film coated, listed with the FDA by Aurobindo Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.

Aurobindo Pharma Limited, NDC labeler code 59651. 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 and famotidine?

18 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ibuprofen and famotidine NDC 59651-908

NDC codes

FDA NDC Directory

Product NDC (as listed)59651-908Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59651-0908Add 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	Copy
59651-908-90	5965109089059651090890	90 TABLET, FILM COATED in 1 BOTTLE (59651-908-90)Marketed from Jun 30, 2025

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 and famotidine
Generic name (nonproprietary): ibuprofen and famotidine
Active ingredients: Ibuprofen — 800 mg/1Famotidine — 26.6 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Aurobindo Pharma LimitedNDC labeler code 59651
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219538
Marketing start: Jun 30, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 59651-908_21688404-41fb-487e-8ba0-aea4431a42faSPL ID 21688404-41fb-487e-8ba0-aea4431a42faSPL set ID 21688404-41fb-487e-8ba0-aea4431a42faRxCUI 1100066UNII WK2XYI10QM, 5QZO15J2Z8UPC 0359651908907
Pharmacologic class: Histamine-2 Receptor Antagonist; 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

N459651090890 followed by a unit qualifier and the quantity

Package 59651-0908-90. 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 Jul 3, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Ibuprofen and famotidine tablet, a combination of the NSAID ibuprofen and the histamine H 2 -receptor antagonist famotidine, is indicated for the relief of signs and symptoms of rheumatoid arthritis and osteoarthritis and to decrease the risk of developing upper gastrointestinal ulcers, which in the clinical trials was defined as a gastric and/or duodenal ulcer, in patients who are taking ibuprofen for those indications. The clinical trials primarily enrolled patients less than 65 years of age without a prior history of gastrointestinal ulcer. Controlled trials do not extend beyond 6 months [see Clinical Studies (14) , Use in Specific Populations (8.5) ] . Ibuprofen and famotidine tablet, a …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59651-908

What is NDC 59651-908?: 59651-908 is the product NDC for Ibuprofen and famotidine, Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 tablet, film coated, listed with the FDA by Aurobindo Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ibuprofen and famotidine.
What is the active ingredient?: Ibuprofen, Famotidine.
Who is the labeler?: Aurobindo Pharma Limited, NDC labeler code 59651. 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 and famotidine?: 18 other product NDCs are listed under this name. See all Ibuprofen and famotidine 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 and famotidine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ibuprofen and Famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0587	80425-0587-0180425-0587-0280425-0587-03
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4580	70518-4580-00
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8897	68788-8897-09
Ibuprofen and Famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1924	70771-1924-09
Ibuprofen and Famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-214	72578-0214-16
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0422	80425-0422-0180425-0422-0280425-0422-03
Ibuprofen And Famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0384	80425-0384-0180425-0384-0280425-0384-03
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	TabletOral	Par Health USA, LLC	49884-366	49884-0366-09
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0483	80425-0483-0180425-0483-0280425-0483-03
Ibuprofen And Famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-315	31722-0315-90

All 19 Ibuprofen and famotidine NDCs