Ibuprofen and famotidine NDC 68788-8897

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-8897Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-8897Add 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
68788-8897-9	68788889709	90 TABLET, FILM COATED in 1 BOTTLE (68788-8897-9)Marketed from Aug 1, 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 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: Preferred Pharmaceuticals Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211890
Marketing start: Aug 1, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 68788-8897_e2f29ca9-9ec8-4b82-8c80-8628d9e3ab2fSPL ID e2f29ca9-9ec8-4b82-8c80-8628d9e3ab2fSPL set ID e2f29ca9-9ec8-4b82-8c80-8628d9e3ab2fRxCUI 1100066UNII WK2XYI10QM, 5QZO15J2Z8
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

N468788889709 followed by a unit qualifier and the quantity

Package 68788-8897-09. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 211890

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

FDA NDC Directory listings under ANDA 211890
Product	Strength	Form · route	Labeler	Product NDC
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-8891
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	PHOENIX RX LLC	85509-1010
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	PHOENIX RX LLC	85509-1626
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4580
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-626
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	Asclemed USA, Inc.	76420-891
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	Doc Rx	69306-266
Ibuprofen and famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0422
Ibuprofen Famotidine	Ibuprofen 800 mg/1; Famotidine 26.6 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-641