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General MedicationsOPHTHALMICGeneric

NEO-DELTA-CORTEF

NEOMYCIN SULFATE; PREDNISOLONE ACETATE

Standard Dose
EQ 3.5MG BASE/GM;0.5%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview NEO-DELTA-CORTEF is listed in Drugs@FDA under application 061039 (ANDA).

Marketing status: Discontinued Active ingredient NEOMYCIN SULFATE; PREDNISOLONE ACETATE Form and strength OINTMENT;OPHTHALMIC - EQ 3.5MG BASE/GM;0.5% Sponsor PHARMACIA AND UPJOHN Submission history See approval history documents.

Structured Monograph

Clinical summary

Approval overview NEO-DELTA-CORTEF is listed in Drugs@FDA under application 061039 (ANDA). Marketing status: Discontinued Active ingredient NEOMYCIN SULFATE; PREDNISOLONE ACETATE Form and strength OINTMENT;OPHTHALMIC - EQ 3.5MG BASE/GM;0.5% Sponsor PHARMACIA AND UPJOHN Submission history See approval history documents.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.