General MedicationsORALGeneric

BUTABARBITAL SODIUM

Standard Dose

48.6MG

Max Dose

Refer to approved labeling

Primary Use

Marketing status: Discontinued

Summary

Approval overview BUTABARBITAL SODIUM is listed in Drugs@FDA under application 083897 (ANDA).

Marketing status: Discontinued Active ingredient BUTABARBITAL SODIUM Form and strength TABLET;ORAL - 48.6MG 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 083897 (ANDA). Marketing status: Discontinued Active ingredient BUTABARBITAL SODIUM Form and strength TABLET;ORAL - 48.6MG 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.