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General MedicationsORALGeneric

PHRENILIN

ACETAMINOPHEN; BUTALBITAL

Standard Dose
325MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview PHRENILIN is listed in Drugs@FDA under application 087811 (ANDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient ACETAMINOPHEN; BUTALBITAL Form and strength TABLET;ORAL - 325MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALEANT Submission history Latest submission status date: 2014-12-13 00:00:00.

Structured Monograph

Clinical summary

Approval overview PHRENILIN is listed in Drugs@FDA under application 087811 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient ACETAMINOPHEN; BUTALBITAL Form and strength TABLET;ORAL - 325MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALEANT Submission history Latest submission status date: 2014-12-13 00:00:00. Submission type: SUPPL.

Monitoring

  • Marketing status: Discontinued
  • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.