NDC codes

FDA NDC Directory
Product NDC (as listed)70518-1345Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-1345Add 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
70518-1345-07051813450090 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1345-0)Marketed from Aug 6, 2018
70518-1345-170518134501100 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1345-1)Marketed from Sep 26, 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)
Olmesartan Medoxomil
Generic name (nonproprietary)
olmesartan medoxomil
Active ingredients
Olmesartan medoxomil — 40 mg/1
Dosage form
Tablet, Coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206763
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 70518-1345_48e9050a-8eab-52eb-e063-6294a90a9d8fSPL ID 48e9050a-8eab-52eb-e063-6294a90a9d8fSPL set ID 33429d86-878e-4e1e-a940-70a8a56a15eaRxCUI 349405UNII 6M97XTV3HD

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

N470518134500 followed by a unit qualifier and the quantity

Package 70518-1345-00. 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

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

Other NDCs under ANDA 206763

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

FDA NDC Directory listings under ANDA 206763
ProductStrengthForm · routeLabelerProduct NDC
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-2749
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, CoatedOralA-S Medication Solutions50090-3655
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, CoatedOralA-S Medication Solutions50090-3656
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7872
Olmesartan MedoxomilOlmesartan medoxomil 5 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-2600
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, CoatedOralAscend Laboratories, LLC67877-446
Olmesartan MedoxomilOlmesartan medoxomil 5 mg/1Tablet, CoatedOralAscend Laboratories, LLC67877-445
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, CoatedOralAscend Laboratories, LLC67877-447
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7087
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-2448
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, CoatedOralProficient Rx LP71205-458
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, CoatedOralREMEDYREPACK INC.70518-1343
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, CoatedOralProficient Rx LP71205-459

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