NDC 65193-180 Ephed Plus Liquid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 65193-180?
What are the uses for Ephed Plus Liquid?
Which are Ephed Plus Liquid UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPHEDRINE HYDROCHLORIDE (UNII: NLJ6390P1Z)
- EPHEDRINE (UNII: GN83C131XS) (Active Moiety)
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Ephed Plus Liquid 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:
- WATER (UNII: 059QF0KO0R)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- MALIC ACID (UNII: 817L1N4CKP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Ephed Plus Liquid?
- RxCUI: 1988809 - ePHEDrine HCl 25 MG / guaiFENesin 400 MG in 60 mL Oral Solution
- RxCUI: 1988809 - ephedrine hydrochloride 0.417 MG/ML / guaifenesin 6.67 MG/ML Oral Solution
- RxCUI: 1988809 - ephedrine HCl 25 MG / guaifenesin 400 MG per 60 ML Oral Solution
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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".