NDC 54868-6306 Bupropion Hydrochloride SR
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6306 - Bupropion Hydrochloride
Product Characteristics
PURPLE (C48327)
PINK (C48328)
11 MM
E;OVER;415
E;ON;ONE;SIDE;AND;1111;ON;OTHER;SIDE
Product Packages
NDC Code 54868-6306-0
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-6306?
What are the uses for Bupropion Hydrochloride SR?
Which are Bupropion Hydrochloride SR 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 SR 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Bupropion Hydrochloride SR?
- 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".