NDC 61919-670 Methadone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61919 - Direct Rx
- 61919-670 - Methadone Hydrochloride
Product Characteristics
Product Packages
NDC Code 61919-670-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 61919-670-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 61919-670-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 61919-670?
What are the uses for Methadone Hydrochloride?
Which are Methadone Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHADONE HYDROCHLORIDE (UNII: 229809935B)
- METHADONE (UNII: UC6VBE7V1Z) (Active Moiety)
Which are Methadone 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Methadone Hydrochloride?
- RxCUI: 864706 - methadone HCl 10 MG Oral Tablet
- RxCUI: 864706 - methadone hydrochloride 10 MG Oral Tablet
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Patient Education
Methadone
Methadone is used to relieve severe pain in people who are expected to need pain medication around the clock for a long time and who cannot be treated with other medications. It also is used to prevent withdrawal symptoms in patients who were addicted to opiate drugs and are enrolled in treatment programs in order to stop taking or continue not taking the drugs. Methadone is in a class of medications called opiate (narcotic) analgesics. Methadone works to treat pain by changing the way the brain and nervous system respond to pain. It works to treat people who were addicted to opiate drugs by producing similar effects and preventing withdrawal symptoms in people who have stopped using these drugs.
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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".