Ziprasidone Hydrochloride
- Product NDC
- 50436-0331
- 11-digit product format
- 504360331
- Labeler code
- 50436
- Product ID
- 50436-0331_b89686a0-da68-41b6-995c-272cc44a3540
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077560
- Marketing category
- ANDA
- Marketing start
- 2012-03-02
- Marketing end
- 0000-00-00
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record