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64679-763 NDC - MIDAZOLAM HYDROCHLORIDE ()

Drug Information

Product NDC: 64679-763

Proprietary Name: Midazolam hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Wockhardt USA LLC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/30/2008

Package Information

No. Package Code Package Description Billing Unit
164679-763-0110 VIAL in 1 CARTON (64679-763-01) / 1 mL in 1 VIAL (64679-763-09)
264679-763-0210 VIAL in 1 CARTON (64679-763-02) / 2 mL in 1 VIAL (64679-763-10)
364679-763-0310 VIAL in 1 CARTON (64679-763-03) / 5 mL in 1 VIAL (64679-763-11)
464679-763-0410 VIAL in 1 CARTON (64679-763-04) / 10 mL in 1 VIAL (64679-763-12)ML
564679-763-0525 VIAL in 1 CARTON (64679-763-05) / 1 mL in 1 VIAL (64679-763-09)
664679-763-0625 VIAL in 1 CARTON (64679-763-06) / 2 mL in 1 VIAL (64679-763-10)
764679-763-0725 VIAL in 1 CARTON (64679-763-07) / 5 mL in 1 VIAL (64679-763-11)
864679-763-0825 VIAL in 1 CARTON (64679-763-08) / 10 mL in 1 VIAL (64679-763-12)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64679-763The 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 NAMEMidazolam 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 DATE5/30/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWockhardt USA LLC.Name 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
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