NDC 51293-691 Phenobarbital
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51293 - Eci Pharmaceuticals, Llc
- 51293-691 - Phenobarbital
Product Characteristics
Product Packages
NDC Code 51293-691-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
Price per Unit: $0.11918 per EA
NDC Code 51293-691-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC
Price per Unit: $0.11918 per EA
NDC Code 51293-691-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 51293-691?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Phenobarbital?
- RxCUI: 198083 - PHENobarbital 100 MG Oral Tablet
- RxCUI: 198083 - phenobarbital 100 MG Oral Tablet
- RxCUI: 198089 - PHENobarbital 60 MG Oral Tablet
- RxCUI: 198089 - phenobarbital 60 MG Oral Tablet
- RxCUI: 312357 - PHENobarbital 15 MG Oral Tablet
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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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[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".