FDA
Nicardipine Hydrochloride
The FDA lists this product in 33 strengths and forms.
Composition
- Active ingredients
- NICARDIPINE HYDROCHLORIDE 30MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- NICARDIPINE HYDROCHLORIDE 25MG/10ML (2.5MG/ML) · InjectableANDA217548-001 · Prescription
- NICARDIPINE HYDROCHLORIDE 30MG · CapsuleANDA217555-002 · Prescription
- NICARDIPINE HYDROCHLORIDE 20MG · CapsuleANDA217555-001 · Prescription
- NICARDIPINE HYDROCHLORIDE 30MG · CapsuleANDA218638-002 · Discontinued
- NICARDIPINE HYDROCHLORIDE 20MG · CapsuleANDA218638-001 · Discontinued
- NICARDIPINE HYDROCHLORIDE 30MG · CapsuleANDA218202-002 · Prescription
- NICARDIPINE HYDROCHLORIDE 20MG · CapsuleANDA218202-001 · Prescription
- NICARDIPINE HYDROCHLORIDE 25MG/10ML (2.5MG/ML) · InjectableANDA090534-001 · Prescription
- NICARDIPINE HYDROCHLORIDE 20MG · CapsuleANDA215377-001 · Prescription
- NICARDIPINE HYDROCHLORIDE 30MG · CapsuleANDA215377-002 · Prescription
- NICARDIPINE HYDROCHLORIDE 25MG/10ML (2.5MG/ML) · Injectable
At a glance
- Brand name
- Nicardipine Hydrochloride
- Route
- Oral
- Dosage form
- Capsule
- Applicant
- Pharmobedient
- Status
- Discontinued
- FDA approval
- 18 Jul 1996
- Application
- ANDA074642-002