NDC 67467-623 Albumin (human)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67467 - Octapharma Pharmazeutika Produktionsgesellschaft M.b.h.
- 67467-623 - Albumin (human)
Product Packages
NDC Code 67467-623-01
Package Description: 100 mL in 1 BOTTLE, GLASS
NDC Code 67467-623-02
Package Description: 250 mL in 1 BOTTLE, GLASS
NDC Code 67467-623-03
Package Description: 500 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 67467-623?
What are the uses for Albumin (human)?
Which are Albumin (human) UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALBUMIN (HUMAN) (UNII: ZIF514RVZR)
- ALBUMIN (HUMAN) (UNII: ZIF514RVZR) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Albumin (human)?
- RxCUI: 1741410 - albumin human 5 % in 100 ML Injection
- RxCUI: 1741410 - 100 ML albumin human, USP 50 MG/ML Injection
- RxCUI: 1741410 - albumin human 5 % per 100 ML Injection
- RxCUI: 1741410 - albumin human 5 GM per 100 ML Injection
- RxCUI: 1741420 - albumin human 5 % in 250 ML Injection
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".