APOMORPHINE HYDROCHLORIDE
APOMORPHINE HYDROCHLORIDE
Approval overview APOMORPHINE HYDROCHLORIDE is listed in Drugs@FDA under application 212025 (ANDA).
Review priority: STANDARD Marketing status: Prescription Active ingredient APOMORPHINE HYDROCHLORIDE Form and strength INJECTABLE;SUBCUTANEOUS - 30MG/3ML (10MG/ML) Sponsor TP ANDA HOLDINGS Submission history Latest submission status date: 2022-02-23 00:00:00.
Structured Monograph
Clinical summary
Approval overview APOMORPHINE HYDROCHLORIDE is listed in Drugs@FDA under application 212025 (ANDA). Review priority: STANDARD Marketing status: Prescription Active ingredient APOMORPHINE HYDROCHLORIDE Form and strength INJECTABLE;SUBCUTANEOUS - 30MG/3ML (10MG/ML) Sponsor TP ANDA HOLDINGS Submission history Latest submission status date: 2022-02-23 00:00:00. Submission type: ORIG.
Monitoring
- • Marketing status: Prescription
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.