Prescription drug · ANDA

Olmesartan Medoxomil NDC 50090-4451

Olmesartan medoxomil 40 mg/1 · Tablet, Film coated · Oral · A-S Medication Solutions

NDC codes

FDA NDC Directory
Product NDC (as listed)50090-4451Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-4451Add 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
50090-4451-05009044510030 TABLET, FILM COATED in 1 BOTTLE (50090-4451-0)Marketed from Aug 5, 2019
50090-4451-15009044510190 TABLET, FILM COATED in 1 BOTTLE (50090-4451-1)Marketed from Aug 5, 2019

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, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203281
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 50090-4451_aa395339-e57c-4ccc-bc9b-4d5c4a18eecaSPL ID aa395339-e57c-4ccc-bc9b-4d5c4a18eeca

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

N450090445100 followed by a unit qualifier and the quantity

Package 50090-4451-00. 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 203281

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

FDA NDC Directory listings under ANDA 203281
ProductStrengthForm · routeLabelerProduct NDC
Olmesartan MedoxomilOlmesartan medoxomil 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2376
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7810
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, Film coatedOralGlenmark Pharmaceuticals Inc., USA68462-438
Olmesartan MedoxomilOlmesartan medoxomil 5 mg/1Tablet, Film coatedOralGlenmark Pharmaceuticals Inc., USA68462-436
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, Film coatedOralGlenmark Pharmaceuticals Inc., USA68462-437
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6686

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Olmesartan Medoxomil NDC 50090-4451 | Med-Code