68788-6931 : Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Extended Release


NDC: 68788-6931
Labeler: Preferred Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Bupropion Hydrochloride (Xl)
Dosage Form: Oral Tablet, Extended Release
Application #: ANDA206556
Rev. Date: 


Appearance:


Markings: I;13
Shapes:  Capsule
Colors:  White
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:

  • 68788-6931-1: 100 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (68788‑6931‑1)
  • 68788-6931-3: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (68788‑6931‑3)
  • 68788-6931-6: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (68788‑6931‑6)
  • 68788-6931-8: 120 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (68788‑6931‑8)
  • 68788-6931-9: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (68788‑6931‑9)

Active Ingredients:

  • Bupropion Hydrochloride

Dosage Strength:

  • 150 mg

Inactive Ingredients:

  • Hypromellose, Unspecified
  • Microcrystalline Cellulose
  • Povidone, Unspecified
  • Citric Acid Monohydrate
  • Silicon Dioxide
  • Magnesium Stearate
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Talc
  • Titanium Dioxide
  • Sodium Bicarbonate
  • Sodium Lauryl Sulfate
  • Triethyl Citrate

Pharmaceutical Classes:

  • 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.
  • 68788-6809 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Preferred Pharmaceuticals Inc.
  • 68788-7347 Bupropion Hydrochloride (Xl) (Xl) 300 mg Oral Tablet, Extended Release by Preferred Pharmaceuticals Inc.
  • 68788-7479 Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release by Preferred Pharmaceuticals Inc.
  • 68788-7863 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Preferred Pharmaceuticals Inc.
  • 68788-8537 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Preferred Pharmaceuticals Inc.
  • 68788-7509 Bupropion Hydrochloride XL 300 mg Oral Tablet, Extended Release by Preferred Pharmaceuticals, Inc.
  • 68788-7756 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Extended Release by Preferred Pharmaceuticals, Inc.
  • 0527-2415 Bupropion Hydrochloride (Xl) (Xl) 150 mg Oral Tablet, Extended Release by Lannett Company Inc.
  • 0527-2430 Bupropion Hydrochloride (Xl) (Xl) 300 mg Oral Tablet, Extended Release by Lannett Company Inc.
  • 0615-8179 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 0615-8241 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Extended Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 0615-8416 Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release by Ncs Healthcare of Ky, LLC Dba Vangard Labs
  • 0615-8418 Bupropion Hydrochloride XL 300 mg Oral Tablet, Extended Release by Ncs Healthcare of Ky, LLC Dba Vangard Labs
  • 0781-5528 Bupropion Hydrochloride (Xl) (Xl) 150 mg Oral Tablet, Extended Release by Sandoz Inc.
  • 0781-5529 Bupropion Hydrochloride (Xl) (Xl) 300 mg Oral Tablet, Extended Release by Sandoz Inc.
  • 0904-7084 Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release by Major Pharmaceuticals
  • 24979-101 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Extended Release by Twi Pharmaceuticals, Inc.
  • 24979-102 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Twi Pharmaceuticals, Inc.
  • 42806-348 Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release by Epic Pharma, LLC
  • 42806-349 Bupropion Hydrochloride XL 300 mg Oral Tablet, Extended Release by Epic Pharma, LLC
  • More related products ...

NDC QR Code

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NDC 68788-6931 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.