General MedicationsOPHTHALMICGeneric
BENOXINATE HYDROCHLORIDE
BENOXINATE HYDROCHLORIDE
Standard Dose
0.4%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary
Approval overview BENOXINATE HYDROCHLORIDE is listed in Drugs@FDA under application 084149 (ANDA).
Marketing status: Discontinued Active ingredient BENOXINATE HYDROCHLORIDE Form and strength SOLUTION/DROPS;OPHTHALMIC - 0.4% Sponsor SOLA BARNES HIND Submission history Latest submission status date: 1975-01-14 00:00:00.
Structured Monograph
Clinical summary
Approval overview BENOXINATE HYDROCHLORIDE is listed in Drugs@FDA under application 084149 (ANDA). Marketing status: Discontinued Active ingredient BENOXINATE HYDROCHLORIDE Form and strength SOLUTION/DROPS;OPHTHALMIC - 0.4% Sponsor SOLA BARNES HIND Submission history Latest submission status date: 1975-01-14 00:00:00. Submission type: ORIG.
Monitoring
- • Marketing status: Discontinued
Interaction Notes
- No interaction notes stored yet.