NDC 70166-536 Phenobarbital
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70166 - Lohxa
- 70166-536 - Phenobarbital
Product Characteristics
Product Packages
NDC Code 70166-536-02
Package Description: 30 BAG in 1 BOX / 1 SYRINGE in 1 BAG / 5 mL in 1 SYRINGE
Product Details
What is NDC 70166-536?
What are the uses for Phenobarbital?
Which are Phenobarbital UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENOBARBITAL (UNII: YQE403BP4D)
- PHENOBARBITAL (UNII: YQE403BP4D) (Active Moiety)
Which are Phenobarbital 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- ALCOHOL (UNII: 3K9958V90M)
- SORBITOL (UNII: 506T60A25R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- ORANGE (UNII: 5EVU04N5QU)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Phenobarbital?
- RxCUI: 702519 - PHENobarbital 20 MG in 5 mL Oral Solution
- RxCUI: 702519 - phenobarbital 4 MG/ML Oral Solution
- RxCUI: 702519 - phenobarbital 20 MG per 5 ML Oral Solution
- RxCUI: 702519 - phenobarbital 30 MG per 7.5 ML Oral Solution
- RxCUI: 702519 - phenobarbital 60 MG per 15 ML Oral Solution
* Please review the disclaimer below.
Patient Education
Phenobarbital
Phenobarbital is used to control seizures. Phenobarbital is also used to relieve anxiety. It is also used to prevent withdrawal symptoms in people who are dependent ('addicted'; feel a need to continue taking the medication) on another barbiturate medication and are going to stop taking the medication. Phenobarbital is in a class of medications called barbiturates. It works by slowing activity in the brain.
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* 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".