75990-576 NDC - PURGO ULTRA FOAM ()

Drug Information

Product NDC: 75990-576

Proprietary Name: Purgo Ultra Foam

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Certus Medical, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/25/2011

Package Information

No. Package Code Package Description Billing Unit
175990-576-011200 mL in 1 CARTRIDGE (75990-576-01)
275990-576-03350 mL in 1 CARTRIDGE (75990-576-03)
375990-576-05540 mL in 1 BOTTLE, PLASTIC (75990-576-05)
475990-576-061 BAG in 1 BOX (75990-576-06) / 800 mL in 1 BAG
575990-576-07700 mL in 1 BAG (75990-576-07)
675990-576-081 BAG in 1 BOX (75990-576-08) / 1000 mL in 1 BAG
775990-576-092000 mL in 1 CARTRIDGE (75990-576-09)
875990-576-101000 mL in 1 CARTRIDGE (75990-576-10)
975990-576-111000 mL in 1 BOTTLE, PLASTIC (75990-576-11)
1075990-576-121000 mL in 1 BAG (75990-576-12)
1175990-576-13800 mL in 1 BAG (75990-576-13)
1275990-576-143785 mL in 1 BOTTLE, PLASTIC (75990-576-14)
1375990-576-15946 mL in 1 BOTTLE, PLASTIC (75990-576-15)
1475990-576-16236 mL in 1 BOTTLE, PLASTIC (75990-576-16)
1575990-576-17532 mL in 1 BOTTLE, PLASTIC (75990-576-17)
1675990-576-1850 mL in 1 BOTTLE, PLASTIC (75990-576-18)
1775990-576-24118 mL in 1 BOTTLE, PLASTIC (75990-576-24)
1875990-576-27800 mL in 1 CARTRIDGE (75990-576-27)
1975990-576-28149 mL in 1 BOTTLE, PLASTIC (75990-576-28)
2075990-576-55208200 mL in 1 DRUM (75990-576-55)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75990-576The 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 NAMEPurgo Ultra FoamThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/25/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECertus Medical, Inc.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