General MedicationsTOPICALStandard

AMMONIUM LACTATE

Standard Dose

EQ 12% BASE

Max Dose

Refer to approved labeling

Primary Use

Marketing status: Prescription

Summary

Approval overview AMMONIUM LACTATE is listed in Drugs@FDA under application 076216 (ANDA).

Marketing status: Prescription Active ingredient AMMONIUM LACTATE Form and strength LOTION;TOPICAL - EQ 12% BASE Sponsor SUN PHARMA CANADA Submission history Latest submission status date: 2004-05-28 00:00:00.

Structured Monograph

Clinical summary

Approval overview AMMONIUM LACTATE is listed in Drugs@FDA under application 076216 (ANDA). Marketing status: Prescription Active ingredient AMMONIUM LACTATE Form and strength LOTION;TOPICAL - EQ 12% BASE Sponsor SUN PHARMA CANADA Submission history Latest submission status date: 2004-05-28 00:00:00. Submission type: ORIG.

Monitoring

• Marketing status: Prescription

Interaction Notes

No interaction notes stored yet.