61786-089 : Bupropion Hydrochloride 100 mg Oral Tablet, Film Coated


NDC: 61786-089
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Bupropion Hydrochloride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA076143
Rev. Date: 


Appearance:


Markings: APO;BUP;100
Shapes:  Round
Colors:  Purple
Size (mm): 9
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.

APO BUP 100: (60505-0157) Bupropion Hydrochloride 100 mg Oral Tablet, Film Coated 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:

  • 61786-089-02: 30 TABLET, FILM COATED IN 1 BLISTER PACK (61786‑089‑02)
  • 61786-089-19: 90 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (61786‑089‑19)

Active Ingredients:

  • Bupropion Hydrochloride

Dosage Strength:

  • 100 mg

Inactive Ingredients:

  • Hydroxypropyl Cellulose
  • Magnesium Stearate
  • Hypromelloses
  • Methylcellulose (100 Cps)
  • Polyethylene Glycols
  • Crospovidone
  • D&c Red No. 7
  • Silicon Dioxide
  • Fumaric Acid
  • Titanium Dioxide

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.
  • 61786-006 Bupropion Hydrochloride 150 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 61786-015 Bupropion Hydrochloride 100 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 61786-021 Bupropion Hydrochloride 100 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 61786-073 Bupropion Hydrochloride 150 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 61786-086 Bupropion Hydrochloride 75 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 61786-243 Bupropion Hydrochloride 100 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 61786-498 Bupropion Hydrochloride 100 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 61786-534 Bupropion Hydrochloride 150 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 61786-536 Bupropion Hydrochloride 150 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 61786-676 Bupropion Hydrochloride 200 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 61786-703 Bupropion Hydrochloride 150 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 61786-733 Bupropion Hydrochloride 150 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 61786-763 Bupropion Hydrochloride 200 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 24236-543 Bupropion Hydrochloride 100 mg Oral Tablet by Remedyrepack Inc.
  • 49349-222 Bupropion Hydrochloride 100 mg 12 Hr Extended Release Tablet by Remedyrepack Inc.
  • 49349-270 Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Remedyrepack Inc.
  • 49349-340 Bupropion Hydrochloride 100 mg Oral Tablet by Remedyrepack Inc.
  • 49349-497 Bupropion Hydrochloride 100 mg Oral Tablet by Remedyrepack Inc.
  • 49349-652 Bupropion Hydrochloride 75 mg Oral Tablet by Remedyrepack Inc.
  • 49349-653 Bupropion Hydrochloride 75 mg Oral Tablet by Remedyrepack Inc.
  • More related products ...

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 61786-089 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.