NDC 68405-021 Appbutamone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PINK (C48328 - PINK WHITE)
CAPSULE (C48336)
20 MM
;
Code Structure Chart
Product Details
What is NDC 68405-021?
What are the uses for Appbutamone?
Which are Appbutamone UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUPROPION HYDROCHLORIDE (UNII: ZG7E5POY8O)
- BUPROPION (UNII: 01ZG3TPX31) (Active Moiety)
- TYROSINE (UNII: 42HK56048U)
- TYROSINE (UNII: 42HK56048U) (Active Moiety)
Which are Appbutamone 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- GELATIN (UNII: 2G86QN327L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
What is the NDC to RxNorm Crosswalk for Appbutamone?
- RxCUI: 993691 - buPROPion HCl 75 MG Oral Tablet
- RxCUI: 993691 - bupropion hydrochloride 75 MG Oral Tablet
- RxCUI: 993691 - bupropion HCl 75 MG 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".