NDC codes

FDA NDC Directory
Product NDC (as listed)50090-3471Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-3471Add 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
50090-3471-05009034710030 TABLET, FILM COATED in 1 BOTTLE (50090-3471-0)Marketed from Jan 31, 2019
50090-3471-15009034710190 TABLET, FILM COATED in 1 BOTTLE (50090-3471-1)Marketed from Jun 11, 2018

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 — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207662
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 50090-3471_51e76f8d-24bc-4ae8-abc7-9f3af7889146SPL ID 51e76f8d-24bc-4ae8-abc7-9f3af7889146SPL set ID b55b6172-d986-4fd9-ba85-a8393c908949RxCUI 349401UNII 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

N450090347100 followed by a unit qualifier and the quantity

Package 50090-3471-00. 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 207662

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

FDA NDC Directory listings under ANDA 207662
ProductStrengthForm · routeLabelerProduct NDC
olmesartan medoxomilOlmesartan medoxomil 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6606
olmesartan medoxomilOlmesartan medoxomil 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0775
olmesartan medoxomilOlmesartan medoxomil 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-9426
olmesartan medoxomilOlmesartan medoxomil 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0817
Olmesartan MedoxomilOlmesartan medoxomil 5 mg/1Tablet, Film coatedOralDirect_Rx72189-373
olmesartan medoxomilOlmesartan medoxomil 20 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-321
olmesartan medoxomilOlmesartan medoxomil 5 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-320
olmesartan medoxomilOlmesartan medoxomil 40 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-322
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, Film coatedOraldirect rx72189-137
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, Film coatedOraldirect rx72189-138
olmesartan medoxomilOlmesartan medoxomil 40 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-3487

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