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Ondansetron hydrochloride - Medication Information

Product NDC Code 65862-188
Drug Name

Ondansetron hydrochloride

Type Generic
Active Ingredients
Ondansetron hydrochloride 8 mg/1
Dosage Form TABLET, FILM COATED
Labeler Name Aurobindo Pharma Limited
Packages
Package NDC Code Description
65862-188-59 5000 tablet, film coated in 1 bag (65862-188-59)
65862-188-03 1 blister pack in 1 carton (65862-188-03) / 3 tablet, film coated in 1 blister pack
65862-188-05 500 tablet, film coated in 1 bottle (65862-188-05)
65862-188-10 10 blister pack in 1 carton (65862-188-10) / 10 tablet, film coated in 1 blister pack
65862-188-30 30 tablet, film coated in 1 bottle (65862-188-30)
65862-188-99 1000 tablet, film coated in 1 bottle (65862-188-99)
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Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API