52125-508 : Bupropion Hydrochloride XL 300 mg 24 Hr Extended Release Tablet


NDC52125-508
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Bupropion Hydrochloridexl XL
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: ANDA077715
Rev. Date: 


Appearance:


Markings: WPI;3332
Shapes:  Round
Colors:  White
Size (mm): 10
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.

WPI 3332: (0591-3332) Bupropion Hydrochloride XL 300 mg 24 Hr Extended Release Tablet by Remedyrepack Inc.
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 52125-508-02: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 VIAL (52125‑508‑02)

Active Ingredients:

  • Bupropion Hydrochloride

Dosage Strength:

  • 300 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Hydroxypropyl Cellulose
  • Colloidal Silicon Dioxide
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Triethyl Citrate
  • Ethylcelluloses
  • Talc
  • Stearic Acid
  • Hydrochloric Acid
  • Titanium Dioxide

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 52125-508 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.