49349-222 : Bupropion Hydrochloride 100 mg 12 Hr Extended Release Tablet


NDC: 49349-222
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Bupropion Hydrochloride
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: ANDA079095
Rev. Date: 


Appearance:


Markings: WPI;858
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 858: (0591-3540) Bupropion Hydrochloride 100 mg 12 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:

  • 49349-222-02: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK (49349‑222‑02)
  • 49349-222-28: 300 TABLET, FILM COATED, EXTENDED RELEASE IN 1 CANISTER (49349‑222‑28)

Active Ingredients:

  • Bupropion Hydrochloride

Dosage Strength:

  • 100 mg

Inactive Ingredients:

  • Hydroxypropyl Cellulose (Type H)
  • Cellulose, Microcrystalline
  • Colloidal Silicon Dioxide
  • Stearic Acid
  • Magnesium Stearate
  • Hydrochloric Acid
  • Lactose Monohydrate
  • Titanium Dioxide
  • Polyethylene Glycols
  • Hydroxypropyl Cellulose
  • Cellulose, Microcrystalline
  • Silicon Dioxide
  • Stearic Acid
  • Magnesium Stearate
  • Hydrochloric Acid
  • Lactose Monohydrate
  • Titanium Dioxide
  • Polyethylene Glycol

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.
  • 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.
  • 49349-704 Bupropion Hydrochloride 100 mg Oral Tablet by Remedyrepack Inc.
  • 49349-726 Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Remedyrepack Inc.
  • 49349-774 Bupropion Hydrochloride 100 mg Oral Tablet by Remedyrepack Inc.
  • 49349-894 Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Remedyrepack Inc.
  • 24236-543 Bupropion Hydrochloride 100 mg Oral Tablet by Remedyrepack Inc.
  • 52125-211 Bupropion Hydrochloride 100 mg 12 Hr Extended Release Tablet by Remedyrepack Inc.
  • 52125-556 Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Remedyrepack Inc.
  • 52125-814 Bupropion Hydrochloride 150 mg/1 Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 52125-882 Bupropion Hydrochloride 100 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 52125-982 Bupropion Hydrochloride 150 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 52125-991 Bupropion Hydrochloride 150 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 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.
  • More related products ...

NDC QR Code

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

NDC 49349-222 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.