Ziprasidone Hydrochloride
- Product NDC
- 70518-1716
- 11-digit product format
- 705181716
- Labeler code
- 70518
- Product ID
- 70518-1716_962fcd27-8c39-4f37-e053-2995a90af8ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077560
- Marketing category
- ANDA
- Marketing start
- 2018-12-07
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record