42192-520 : Quadrapax Oral Elixir


NDC: 42192-520
Labeler: Acella Pharmaceuticals, LLC
Product Type: Human Prescription Drug
Drug Name: Quadrapax
Dosage Form: Oral Elixir
Rev. Date: 
CSA Schedule: CIV (US) [1]


[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 42192-520-16: 473 ML IN 1 BOTTLE (42192‑520‑16)

Active Ingredients:

  • Atropine Sulfate
  • Hyoscyamine Sulfate
  • Phenobarbital
  • Scopolamine Hydrobromide

Dosage Strength:

  • .0194 mg/5mL
  • .1037 mg/5mL
  • 16.2 mg/5mL
  • .0065 mg/5mL

Pharmaceutical Classes:

  • Anticholinergic [EPC]
  • Cholinergic Antagonists [MoA]
  • Cholinergic Muscarinic Antagonist [EPC]
  • Cholinergic Muscarinic Antagonists [MoA]

Related Products:

Based on records with the same trade name.
  • 21695-970 Quadrapax Oral Elixir by Rebel Distributors Corp

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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.