OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 12.5 mg / 1; 20 mg / 1 Tablet 30 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

NDC 1150090-7478-00
Product NDC50090-7478
Generic Drug NameOLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Brand NameOLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
ManufacturerA-S Medication Solutions
Strength12.5 mg / 1; 20 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Film Coated
Package Description30 TABLET, FILM COATED in 1 BOTTLE (50090-7478-0)
Active IngredientsHydrochlorothiazide; Olmesartan Medoxomil
Marketing CategoryANDA

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NDC snapshot

OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 12.5 mg / 1; 20 mg / 1 Tablet is tracked under NDC 50090-7478-00 and rolls up into product family 50090-7478. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Film Coated.
  • Manufacturer: A-S Medication Solutions.
  • Dosage form: Tablet.
  • Family size: 2 indexed presentations.

Official references

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Alternate presentations in this family

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Potential alternatives with matching presentation

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View Potential Alternative HubOlmesartan medoxomil and hydrochlorothiazide 12.5 mg / 1; 20 mg / 1 Tablet 30 Tablet, Film Coated Bottle10 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 12.5 mg / 1; 20 mg / 1 Tablet 30 Tablet, Film Coated, NDC 50090-7478-00, is a A-S Medication Solutions 12.5 mg / 1; 20 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.

NDC search formats

  • Canonical NDC 11: 50090-7478-00
  • Digits-only NDC 11: 50090747800
  • Possible 10-digit display format: 50090-7478-0 (5009074780)

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