ziprasidone hydrochloride
- Product NDC
- 0615-7703
- 11-digit product format
- 006157703
- Labeler code
- 0615
- Product ID
- 0615-7703_31523ae2-b4b1-4691-bb0c-f581782a33b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA077565
- Marketing category
- ANDA
- Marketing start
- 2012-03-02
- Marketing end
- 0000-00-00
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 80 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#