67777-100 NDC - POVIDONE IODINE ()

Drug Information

Product NDC: 67777-100

Proprietary Name: povidone iodine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Dynarex Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/3/2002

Package Information

No. Package Code Package Description Billing Unit
167777-100-0148 BOTTLE in 1 CASE (67777-100-01) / 118 mL in 1 BOTTLEML
267777-100-0224 BOTTLE in 1 CASE (67777-100-02) / 237 mL in 1 BOTTLEML
367777-100-0324 BOTTLE in 1 CASE (67777-100-03) / 474 mL in 1 BOTTLEML
467777-100-0412 BOTTLE in 1 CASE (67777-100-04) / 946 mL in 1 BOTTLE
567777-100-054 BOTTLE in 1 CASE (67777-100-05) / 3784 mL in 1 BOTTLEML
667777-100-0648 BOTTLE in 1 CASE (67777-100-06) / 59 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC67777-100The 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 NAMEpovidone iodineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/3/2002This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDynarex CorporationName 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