Olmesartan Medoxomil And Hydrochlorothiazide NDC 70518-4577

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4577Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4577Add 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
70518-4577-0	70518457700	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4577-0)Marketed from Feb 27, 2026

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): Olmesartan Medoxomil And Hydrochlorothiazide
Generic name (nonproprietary): olmesartan medoxomil and hydrochlorothiazide
Active ingredients: Olmesartan medoxomil — 40 mg/1Hydrochlorothiazide — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207037
Marketing start: Feb 27, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers: Product ID 70518-4577_5baf9a88-d4ab-2513-e063-6394a90a0187SPL ID 5baf9a88-d4ab-2513-e063-6394a90a0187
Pharmacologic class: Angiotensin 2 Receptor Blocker; Thiazide Diuretic

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

N470518457700 followed by a unit qualifier and the quantity

Package 70518-4577-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 207037

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

FDA NDC Directory listings under ANDA 207037
Product	Strength	Form · route	Labeler	Product NDC
Olmesartan Medoxomil And Hydrochlorothiazide	Olmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-451
Olmesartan Medoxomil And Hydrochlorothiazide	Olmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-452
Olmesartan Medoxomil And Hydrochlorothiazide	Olmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-453