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General MedicationsORALGeneric

SODIUM BUTABARBITAL

BUTABARBITAL SODIUM

Standard Dose
100MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview SODIUM BUTABARBITAL is listed in Drugs@FDA under application 085881 (ANDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient BUTABARBITAL SODIUM Form and strength TABLET;ORAL - 100MG Sponsor LANNETT Submission history Latest submission status date: 2019-02-06 00:00:00.

Structured Monograph

Clinical summary

Approval overview SODIUM BUTABARBITAL is listed in Drugs@FDA under application 085881 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient BUTABARBITAL SODIUM Form and strength TABLET;ORAL - 100MG Sponsor LANNETT Submission history Latest submission status date: 2019-02-06 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.
SODIUM BUTABARBITAL (BUTABARBITAL SODIUM) | Drug Monograph | MedicHelpline