ziprasidone hydrochloride
- Product NDC
- 68071-3418
- 11-digit product format
- 680713418
- Labeler code
- 68071
- Product ID
- 68071-3418_2d6c5430-64f8-bbe9-e063-6294a90aed50
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077565
- Marketing category
- ANDA
- Marketing start
- 2012-03-02
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 216X081ORU | ZIPRASIDONE HYDROCHLORIDE | 138982-67-9 | ZIPRASIDONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3418-9 | 68071341809 | 90 CAPSULE in 1 BOTTLE (68071-3418-9) | 90 capsule | 2023-05-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ziprasidone hydrochloride | NuCare Pharmaceuticals,Inc. | 2025-02-05 | HUMAN PRESCRIPTION DRUG LABEL | 3 |