NDC 50383-062 Dextromethorphan Hbr And Guaifenesin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50383 - Akorn
- 50383-062 - Dextromethorphan Hbr And Guaifenesin
Product Characteristics
VANILLA (C73421 - ARTIFICIAL VANILLA FLAVOR)
Product Packages
NDC Code 50383-062-06
Package Description: 4 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY (50383-062-05) / 5 mL in 1 CUP, UNIT-DOSE
NDC Code 50383-062-07
Package Description: 10 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE
NDC Code 50383-062-11
Package Description: 4 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY (50383-062-10) / 10 mL in 1 CUP, UNIT-DOSE
NDC Code 50383-062-12
Package Description: 10 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE
Product Details
What is NDC 50383-062?
What are the uses for Dextromethorphan Hbr And Guaifenesin?
Which are Dextromethorphan Hbr And Guaifenesin UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Dextromethorphan Hbr And Guaifenesin 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:
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- ASPARTAME (UNII: Z0H242BBR1)
- HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
What is the NDC to RxNorm Crosswalk for Dextromethorphan Hbr And Guaifenesin?
- RxCUI: 996520 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Solution
- RxCUI: 996520 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Solution
- RxCUI: 996520 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral Solution
- RxCUI: 996520 - dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral Solution
- RxCUI: 996520 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 10 ML Oral Solution
* Please review the disclaimer below.
Patient Education
Dextromethorphan
Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.
[Learn More]
Guaifenesin
Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
[Learn More]
* Please review the disclaimer below.
[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".