General MedicationsINJECTIONGeneric

PROMETHAZINE HYDROCHLORIDE

Standard Dose

25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Max Dose

Refer to approved labeling

Primary Use

Marketing status: Discontinued

Summary

Approval overview PROMETHAZINE HYDROCHLORIDE is listed in Drugs@FDA under application 040454 (ANDA).

Marketing status: Discontinued Active ingredient PROMETHAZINE HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor TEVA PHARMS USA Submission history Latest submission status date: 2009-10-20 00:00:00.

Structured Monograph

Clinical summary

Approval overview PROMETHAZINE HYDROCHLORIDE is listed in Drugs@FDA under application 040454 (ANDA). Marketing status: Discontinued Active ingredient PROMETHAZINE HYDROCHLORIDE Form and strength INJECTABLE;INJECTION - 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor TEVA PHARMS USA Submission history Latest submission status date: 2009-10-20 00:00:00. Submission type: SUPPL.

Monitoring

• Marketing status: Discontinued

Interaction Notes

No interaction notes stored yet.