General MedicationsOPHTHALMICGeneric
GARAMYCIN
GENTAMICIN SULFATE
Standard Dose
EQ 0.3% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
Key Takeaways
- Primary indication: Marketing status: Discontinued
- Approval overview GARAMYCIN is listed in Drugs@FDA under application 050039 (NDA).
- Marketing status: Discontinued Active ingredient GENTAMICIN SULFATE Form and strength SOLUTION/DROPS;OPHTHALMIC - EQ 0.3% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SCHERING Submission history Latest submission status date: 1999-10-18 00:00:00.
Structured Monograph
Clinical summary
Approval overview GARAMYCIN is listed in Drugs@FDA under application 050039 (NDA). Marketing status: Discontinued Active ingredient GENTAMICIN SULFATE Form and strength SOLUTION/DROPS;OPHTHALMIC - EQ 0.3% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SCHERING Submission history Latest submission status date: 1999-10-18 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
Interaction Notes
- No interaction notes stored yet.