NDC 50090-4518 Hydralazine Hydrochloride
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What is NDC 50090-4518?
What are the uses for Hydralazine Hydrochloride?
Which are Hydralazine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDRALAZINE HYDROCHLORIDE (UNII: FD171B778Y)
- HYDRALAZINE (UNII: 26NAK24LS8) (Active Moiety)
Which are Hydralazine Hydrochloride Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Hydralazine Hydrochloride?
- RxCUI: 966571 - hydrALAZINE HCl 20 MG in 1 ML Injection
- RxCUI: 966571 - 1 ML hydralazine hydrochloride 20 MG/ML Injection
- RxCUI: 966571 - hydralazine HCl 20 MG per 1 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".