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General MedicationsORALGeneric

BUTABARBITAL SODIUM

BUTABARBITAL SODIUM

Standard Dose
97.2MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview BUTABARBITAL SODIUM is listed in Drugs@FDA under application 083896 (ANDA).

Marketing status: Discontinued Active ingredient BUTABARBITAL SODIUM Form and strength TABLET;ORAL - 97.2MG Sponsor SOLVAY Submission history Latest submission status date: 1974-06-21 00:00:00.

Structured Monograph

Clinical summary

Approval overview BUTABARBITAL SODIUM is listed in Drugs@FDA under application 083896 (ANDA). Marketing status: Discontinued Active ingredient BUTABARBITAL SODIUM Form and strength TABLET;ORAL - 97.2MG Sponsor SOLVAY Submission history Latest submission status date: 1974-06-21 00:00:00. Submission type: ORIG.

Monitoring

  • Marketing status: Discontinued

Interaction Notes

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