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Buspirone hydrochloride - Medication Information

Product NDC Code 65841-783
Drug Name

Buspirone hydrochloride

Type Generic
Active Ingredients
Buspirone hydrochloride 15 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 866018,
866083,
866090,
866094,
866111
Application Number ANDA078888
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
65841-783-01 100 tablet in 1 bottle (65841-783-01)
65841-783-05 500 tablet in 1 bottle (65841-783-05)
65841-783-10 1000 tablet in 1 bottle (65841-783-10)
65841-783-14 60 tablet in 1 bottle (65841-783-14)
65841-783-28 180 tablet in 1 bottle (65841-783-28)
65841-783-77 100 blister pack in 1 carton (65841-783-77) / 1 tablet in 1 blister pack (65841-783-30)
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Spl product data elements

Usually a list of ingredients in a drug product.
buspirone hydrochloride buspirone hydrochloride BUSPIRONE HYDROCHLORIDE BUSPIRONE SILICON DIOXIDE LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE SODIUM STARCH GLYCOLATE TYPE A POTATO white to off-white CAPSULE ZE;36 buspirone hydrochloride buspirone hydrochloride BUSPIRONE HYDROCHLORIDE BUSPIRONE SILICON DIOXIDE LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE SODIUM STARCH GLYCOLATE TYPE A POTATO white to off-white CAPSULE ZE;37 buspirone hydrochloride buspirone hydrochloride BUSPIRONE HYDROCHLORIDE BUSPIRONE SILICON DIOXIDE LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE SODIUM STARCH GLYCOLATE TYPE A POTATO white to off-white CAPSULE 5;ZE;38 buspirone hydrochloride buspirone hydrochloride BUSPIRONE HYDROCHLORIDE BUSPIRONE SILICON DIOXIDE LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE SODIUM STARCH GLYCOLATE TYPE A POTATO white to off-white CAPSULE 10;ZE;39 buspirone hydrochloride buspirone hydrochloride BUSPIRONE HYDROCHLORIDE BUSPIRONE SILICON DIOXIDE LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE SODIUM STARCH GLYCOLATE TYPE A POTATO white to off-white CAPSULE 6;23

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 65841-781-01 in bottle of 100 tablets Buspirone Hydrochloride Tablets USP, 5 mg R x only 100 tablets NDC 65841-842-01 in bottle of 100 tablets Buspirone Hydrochloride Tablets USP, 7.5 mg R x only 100 tablets NDC 65841-782-01 in bottle of 100 tablets Buspirone Hydrochloride Tablets USP, 10 mg R x only 100 tablets NDC 65841-783-01 in bottle of 100 tablets Buspirone Hydrochloride Tablets USP, 15 mg R x only 100 tablets NDC 65841-784-14 in bottle of 60 tablets Buspirone Hydrochloride Tablets USP, 30 mg R x only 60 tablets Buspirone Hydrochloride Tablets USP, 5 mg 7.5 mg label Buspirone Hydrochloride Tablets USP, 10 mg Buspirone Hydrochloride Tablets USP, 15 mg Buspirone Hydrochloride Tablets USP, 30 mg

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