49252-101 NDC - BUSPIRONE HYDROCHLORIDE ()

Drug Information

Product NDC: 49252-101

Proprietary Name: BusPIRone Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Inventia Healthcare Private Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/16/2018

Package Information

No. Package Code Package Description Billing Unit
149252-101-1160 TABLET in 1 BOTTLE (49252-101-11)
249252-101-13100 TABLET in 1 BOTTLE (49252-101-13)
349252-101-17500 TABLET in 1 BOTTLE (49252-101-17)
449252-101-181000 TABLET in 1 BOTTLE (49252-101-18)
549252-101-5710 BLISTER PACK in 1 CARTON (49252-101-57) / 10 TABLET in 1 BLISTER PACK (49252-101-54)

NDC Record

Field Name Field Value Definition
PRODUCT NDC49252-101The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEBusPIRone HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/16/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEInventia Healthcare Private LimitedName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023