71269-040 : Tuxarin Oral Tablet, Extended Release


NDC: 71269-040
Labeler: Mainpointe Pharmaceuticals
Product Type: Human Prescription Drug
Drug Name: Tuxarin
Dosage Form: Oral Tablet, Extended Release
Application #: NDA206323
Rev. Date: 
CSA Schedule: CIII (US) [1]


[1] Schedule III / IIIN Controlled Substance: Has a potential for abuse less than substances in Schedules I or II and abuse may lead to moderate or low physical dependence or high psychological dependence. (i.e. Products containing not more than 90 milligrams of Codeine per dosage unit [such as Tylenol with Codeine], other narcotics such as Buprenorphine (Suboxone), and Schedule IIIN non-narcotics such as Didrex, Ketamine, Phendimetrazine, and Anabolic Steroids). More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:


Markings: MP;CC
Shapes:  Round
Colors:  White
Size (mm): 6
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:

  • 71269-040-10: 100 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (71269‑040‑10)
  • 71269-040-30: 100 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (71269‑040‑30)

Active Ingredients:

  • Chlorpheniramine Maleate
  • Codeine Phosphate

Dosage Strength:

  • 8 mg
  • 54.3 mg

Pharmaceutical Classes:

  • Full Opioid Agonists [MoA]
  • Histamine H1 Receptor Antagonists [MoA]
  • Histamine-1 Receptor Antagonist [EPC]
  • Opioid Agonist [EPC]

NDC QR Code

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NDC 71269-040 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.