NDC 68151-0146 Promethazine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-0146 - Promethazine Hydrochloride
Product Characteristics
Product Packages
NDC Code 68151-0146-1
Package Description: 5 mL in 1 SYRINGE, PLASTIC
Product Details
What is NDC 68151-0146?
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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALCOHOL (UNII: 3K9958V90M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Promethazine Hydrochloride?
- RxCUI: 992432 - promethazine HCl 6.25 MG in 5 mL Oral Solution
- RxCUI: 992432 - promethazine hydrochloride 1.25 MG/ML Oral Solution
- RxCUI: 992432 - promethazine HCl 6.25 MG per 5 ML Oral Syrup
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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".