NDC 0440-7200 Bupropion Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0440 - Liberty Pharmaceuticals, Inc.
- 0440-7200 - Bupropion Hydrochloride
Product Characteristics
Product Packages
NDC Code 0440-7200-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 0440-7200-60
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 0440-7200-81
Package Description: 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 0440-7200-90
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 0440-7200-91
Package Description: 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 0440-7200-92
Package Description: 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 0440-7200?
What are the uses for Bupropion Hydrochloride?
Which are Bupropion Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUPROPION HYDROCHLORIDE (UNII: ZG7E5POY8O)
- BUPROPION (UNII: 01ZG3TPX31) (Active Moiety)
Which are Bupropion 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:
- COPOVIDONE (UNII: D9C330MD8B)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROXYPROPYL CELLULOSE (120000 MW) (UNII: UKE75GEA7F)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Bupropion Hydrochloride?
- RxCUI: 993518 - buPROPion HCl 150 MG 12HR Extended Release Oral Tablet
- RxCUI: 993518 - 12 HR bupropion hydrochloride 150 MG Extended Release Oral Tablet
- RxCUI: 993518 - bupropion HCl 150 MG 12 HR Extended Release Oral Tablet
* 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".