NDC 21695-138 Wellbutrin Xl
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-138 - Wellbutrin Xl
Product Characteristics
9 MM
WELLBUTRIN;XL;300
Product Packages
NDC Code 21695-138-15
Package Description: 15 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 21695-138-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 21695-138?
What are the uses for Wellbutrin Xl?
Which are Wellbutrin Xl UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUPROPION HYDROCHLORIDE (UNII: ZG7E5POY8O)
- BUPROPION (UNII: 01ZG3TPX31) (Active Moiety)
Which are Wellbutrin Xl 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:
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- GLYCERYL BEHENATE (UNII: R8WTH25YS2)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Wellbutrin Xl?
- RxCUI: 993541 - buPROPion HCl 150 MG 24HR Extended Release Oral Tablet
- RxCUI: 993541 - 24 HR bupropion hydrochloride 150 MG Extended Release Oral Tablet
- RxCUI: 993541 - bupropion HCl XL 150 MG 24 HR Extended Release Oral Tablet
- RxCUI: 993545 - Wellbutrin XL 150 MG 24HR Extended Release Oral Tablet
- RxCUI: 993545 - 24 HR bupropion hydrochloride 150 MG Extended Release Oral Tablet [Wellbutrin]
* 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".