NDC 55648-102 Bupropion Hydrochloride (xl)
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Product Details
What is NDC 55648-102?
What are the uses for Bupropion Hydrochloride (xl)?
Which are Bupropion Hydrochloride (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 Bupropion Hydrochloride (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:
- AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- POVIDONE (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Bupropion Hydrochloride (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
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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".