24486-200 : Hydrocodone Polistirex and Chlorpheniramine Polistirex Oral Suspension, Extended Release


NDC24486-200
Labeler: Aristos Phamaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-release
Dosage Form: Oral Suspension, Extended Release
Application #: ANDA091671
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:

  • 24486-200-16: 473 ML IN 1 BOTTLE (24486‑200‑16)

Active Ingredients:

  • Chlorpheniramine
  • Hydrocodone

Dosage Strength:

  • 8 mg/5mL
  • 10 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.
  • 17856-0087 Hydrocodone Polistirex and Chlorpheniramine Polistirex Oral Suspension, Extended Release by Atlantic Biologicals Corp.
  • 27808-086 Hydrocodone Polistirex and Chlorpheniramine Polistirex Oral Suspension, Extended Release by Tris Pharma Inc
  • 63629-2303 Hydrocodone Polistirex and Chlorpheniramine Polistirex Oral Suspension, Extended Release by Bryant Ranch Prepack
  • 63629-2304 Hydrocodone Polistirex and Chlorpheniramine Polistirex Oral Suspension, Extended Release by Bryant Ranch Prepack
  • 72162-1283 Hydrocodone Polistirex and Chlorpheniramine Polistirex Oral Suspension, Extended Release by Bryant Ranch Prepack

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.