Olmesartan Medoxomil and Hydrochlorothiazide 12.5 mg / 1; 40 mg / 1 Tablet 10 Blister Pack

Reference details for licensed healthcare facility review and verification.

NDC 1165862-0780-78
Product NDC65862-0780
Generic Drug NameOlmesartan Medoxomil and Hydrochlorothiazide
Brand NameOlmesartan Medoxomil and Hydrochlorothiazide
ManufacturerAurobindo Pharma Limited
Strength12.5 mg / 1; 40 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity10 Blister Pack
Package Description10 BLISTER PACK in 1 CARTON (65862-780-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-780-10)
Active IngredientsHydrochlorothiazide; Olmesartan Medoxomil
Marketing CategoryANDA

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NDC snapshot

Olmesartan Medoxomil and Hydrochlorothiazide 12.5 mg / 1; 40 mg / 1 Tablet is tracked under NDC 65862-0780-78 and rolls up into product family 65862-0780. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 10 Blister Pack.
  • Manufacturer: Aurobindo Pharma Limited.
  • Dosage form: Tablet.
  • Family size: 4 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; 40 mg / 1 Tablet 10 Blister Pack Blister3 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Olmesartan Medoxomil and Hydrochlorothiazide 12.5 mg / 1; 40 mg / 1 Tablet 10 Blister Pack, NDC 65862-0780-78, is a Aurobindo Pharma Limited 12.5 mg / 1; 40 mg / 1 tablet presentation packaged as 10 Blister Pack.

NDC search formats

  • Canonical NDC 11: 65862-0780-78
  • Digits-only NDC 11: 65862078078
  • Possible 10-digit display format: 65862-780-78 (6586278078)

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