NDC 50090-1618 Promethazine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-1618 - Promethazine Hydrochloride
Product Characteristics
Product Packages
NDC Code 50090-1618-0
Package Description: 12 TABLET in 1 BOTTLE
NDC Code 50090-1618-1
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 50090-1618-6
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 50090-1618-9
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 50090-1618?
What are the uses for Promethazine Hydrochloride?
Which are Promethazine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROMETHAZINE HYDROCHLORIDE (UNII: R61ZEH7I1I)
- PROMETHAZINE (UNII: FF28EJQ494) (Active Moiety)
Which are Promethazine 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Promethazine Hydrochloride?
- RxCUI: 992447 - promethazine HCl 25 MG Oral Tablet
- RxCUI: 992447 - promethazine hydrochloride 25 MG Oral Tablet
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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".