52125-926 : Wellbutrin XL 150 mg Oral Tablet, Extended Release


NDC: 52125-926
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Wellbutrin XL Xl
Dosage Form: Oral Tablet, Extended Release
Application #: NDA021515
Rev. Date: 


Appearance:


Markings: WELLBUTRIN;XL;150
Shapes:  Round
Colors:  White
Size (mm): 7
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 52125-926-02: 30 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK (52125‑926‑02)

Active Ingredients:

  • Bupropion Hydrochloride

Dosage Strength:

  • 150 mg

Inactive Ingredients:

  • Ethylcelluloses
  • Povidone
  • Polyethylene Glycols
  • Silicon Dioxide
  • Glyceryl Dibehenate
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Polyvinyl Alcohol
  • Triethyl Citrate

Pharmaceutical Classes:

  • Aminoketone [EPC]
  • Dopamine Uptake Inhibitors [MoA]
  • Increased Dopamine Activity [PE]
  • Increased Norepinephrine Activity [PE]
  • Norepinephrine Uptake Inhibitors [MoA]

NDC QR Code

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NDC 52125-926 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.