50474-150 : Tussionex Pennkinetic Oral Suspension, Extended Release


NDC: 50474-150
Labeler: Ucb Inc.
Product Type: Human Prescription Drug
Drug Name:  Tussionex Pennkinetic
Dosage Form: Oral Suspension, Extended Release
Application #: NDA019111
Rev. Date: 
CSA Schedule: CII (US) [1]


[1] Schedule II / IIN Controlled Substance: High potential for abuse which may lead to severe psychological or physical dependence. (i.e. Narcotics such as Dilaudid, Methadone, Demerol, Oxycodone, Percocet, Fentanyl, Morphine, Opium, Codeine, and Hydrocodone ... Schedule IIN stimulants include non-narcotic Amphetamines such as Dexedrine, Adderall, Desoxyn, Methylphenidate (Ritalin) ... Other Schedule II substances include Amobarbital, Glutethimide, and Pentobarbital. More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 50474-150-49: 1 BOTTLE, PLASTIC IN 1 CARTON (50474‑150‑49) > 115 ML IN 1 BOTTLE, PLASTIC

Active Ingredients:

  • Hydrocodone
  • Chlorpheniramine

Dosage Strength:

  • 10 mg/5mL
  • 8 mg/5mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 53014-548 Tussionex Pennkinetic Oral Suspension, Extended Release by Ucb Manufacturing Inc

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.