68001-236 : Bupropion Hydrochloride 150 mg/1 Oral Tablet, Film Coated, Extended Release


NDC68001-236
Labeler: Bluepoint Laboratories
Product Type: Human Prescription Drug
Drug Name:  Bupropion Hydrochloride XL
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: ANDA077715
Rev. Date: 


Appearance:


Markings: WPI;3331
Shapes:  Round
Colors:  White
Size (mm): 8
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 3331: (0591-3331) Bupropion Hydrochloride 150 mg/1 Oral Tablet, Film Coated, Extended Release by Bluepoint Laboratories
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:

  • 68001-236-03: 500 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (68001‑236‑03)
  • 68001-236-04: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (68001‑236‑04)
  • 68001-236-05: 90 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (68001‑236‑05)

Active Ingredients:

  • Bupropion Hydrochloride

Dosage Strength:

  • 150 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Ethylcelluloses
  • Hydroxypropyl Cellulose (Type H)
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Cellulose, Microcrystalline
  • Stearic Acid
  • Talc
  • Titanium Dioxide
  • Hydrochloric Acid
  • 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.
  • 68001-321 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Bluepoint Laboratories
  • 68001-322 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Extended Release by Bluepoint Laboratories
  • 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
  • 42806-414 Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release by Epic Pharma, LLC
  • 42806-416 Bupropion Hydrochloride XL 300 mg Oral Tablet, Extended Release by Epic Pharma, LLC
  • 43598-655 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Film Coated, Extended Release by Dr Reddys Laboratories Inc
  • 43598-656 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Film Coated, Extended Release by Dr Reddys Laboratories Inc
  • 43826-067 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Extended Release by Bora Pharmaceutical Laboratories Inc.
  • More related products ...

NDC 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.