64764-890 : Contrave Oral Tablet, Film Coated, Extended Release


NDC: 64764-890
Labeler: Takeda Pharmaceuticals America, Inc.
Product Type: Human Prescription Drug
Drug Name:  Contrave
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: NDA200063
Rev. Date: 


Appearance:


Markings: NB;890
Shapes:  Round
Colors:  Blue
Size (mm): 12
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:

  • 64764-890-00: 70 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (64764‑890‑00)
  • 64764-890-99: 120 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (64764‑890‑99)

Active Ingredients:

  • Bupropion Hydrochloride
  • Naltrexone Hydrochloride

Dosage Strength:

  • 90 mg
  • 8 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Hydroxypropyl Cellulose (Type H)
  • Anhydrous Lactose
  • Cysteine Hydrochloride
  • Crospovidone
  • Magnesium Stearate
  • Hypromelloses
  • Edetate Disodium
  • Lactose Monohydrate
  • Silicon Dioxide
  • Fd&c Blue No. 2

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 50090-2868 Contrave Oral Tablet, Film Coated, Extended Release by A-s Medication Solutions

NDC QR Code

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NDC 64764-890 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.