FDA
Cyproheptadine Hydrochloride
The FDA lists this product in 39 strengths and forms.
Composition
- Active ingredients
- CYPROHEPTADINE HYDROCHLORIDE 2MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- CYPROHEPTADINE HYDROCHLORIDE 4MG · TabletANDA088212-001 · Prescription
- CYPROHEPTADINE HYDROCHLORIDE 2MG/5ML · SyrupANDA089199-001 · Discontinued
- CYPROHEPTADINE HYDROCHLORIDE 4MG · TabletANDA207555-001 · Prescription
- CYPROHEPTADINE HYDROCHLORIDE 4MG · TabletANDA208938-001 · Prescription
- CYPROHEPTADINE HYDROCHLORIDE 4MG · TabletANDA040537-001 · Prescription
- CYPROHEPTADINE HYDROCHLORIDE 4MG · TabletANDA040644-001 · Prescription
- CYPROHEPTADINE HYDROCHLORIDE 4MG · TabletANDA089057-001 · Discontinued
- CYPROHEPTADINE HYDROCHLORIDE 2MG/5ML · SyrupANDA203191-001 · Prescription
- CYPROHEPTADINE HYDROCHLORIDE 4MG · TabletANDA206553-001 · Prescription
- CYPROHEPTADINE HYDROCHLORIDE 4MG · Tablet
At a glance
- Brand name
- Cyproheptadine Hydrochloride
- Route
- Oral
- Dosage form
- Syrup
- Applicant
- Actavis Mid Atlantic
- Status
- Discontinued
- FDA approval
- 16 Apr 1980
- Application
- ANDA086833-001