NDC 67046-077 Bupropion Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 67046-077?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FUMARIC ACID (UNII: 88XHZ13131)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Bupropion Hydrochloride?
- RxCUI: 993687 - buPROPion HCl 100 MG Oral Tablet
- RxCUI: 993687 - bupropion hydrochloride 100 MG Oral Tablet
- RxCUI: 993691 - buPROPion HCl 75 MG Oral Tablet
- RxCUI: 993691 - bupropion hydrochloride 75 MG Oral Tablet
- RxCUI: 993691 - bupropion HCl 75 MG Oral Tablet
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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".