Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 5 mg / 1; 12.5 mg / 1; 20 mg / 1 Tablet 30 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

NDC 1149884-0786-11
Product NDC49884-0786
Generic Drug Nameolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Brand Nameolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
ManufacturerEndo USA, Inc.
Strength5 mg / 1; 12.5 mg / 1; 20 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Film Coated
Package Description30 TABLET, FILM COATED in 1 BOTTLE (49884-786-11)
Active IngredientsAmlodipine Besylate; Hydrochlorothiazide; Olmesartan Medoxomil
Marketing CategoryANDA

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NDC snapshot

olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 5 mg / 1; 12.5 mg / 1; 20 mg / 1 Tablet is tracked under NDC 49884-0786-11 and rolls up into product family 49884-0786. 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: Endo USA, Inc..
  • 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 amlodipine besylate and hydrochlorothiazide 5 mg / 1; 12.5 mg / 1; 20 mg / 1 Tablet 30 Tablet, Film Coated Bottle5 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 5 mg / 1; 12.5 mg / 1; 20 mg / 1 Tablet 30 Tablet, Film Coated, NDC 49884-0786-11, is a Endo USA, Inc. 5 mg / 1; 12.5 mg / 1; 20 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.

NDC search formats

  • Canonical NDC 11: 49884-0786-11
  • Digits-only NDC 11: 49884078611
  • Possible 10-digit display format: 49884-786-11 (4988478611)

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