NDC 64725-0737 Bupropion Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-0737 - Bupropion Hydrochloride
Product Characteristics
9 MM
737
Product Packages
NDC Code 64725-0737-1
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 64725-0737?
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:
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- SACCHARIN (UNII: FST467XS7D)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TALC (UNII: 7SEV7J4R1U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
What is the NDC to RxNorm Crosswalk for Bupropion Hydrochloride?
- RxCUI: 993503 - buPROPion HCl 100 MG 12HR Extended Release Oral Tablet
- RxCUI: 993503 - 12 HR bupropion hydrochloride 100 MG Extended Release Oral Tablet
- RxCUI: 993503 - bupropion HCl 100 MG 12 HR Extended Release Oral Tablet
- RxCUI: 993518 - buPROPion HCl 150 MG 12HR Extended Release Oral Tablet
- RxCUI: 993518 - 12 HR bupropion hydrochloride 150 MG 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".