ziprasidone hydrochloride
- Product NDC
- 71335-9761
- 11-digit product format
- 713359761
- Labeler code
- 71335
- Product ID
- 71335-9761_6fd0b930-d288-43ec-850b-e34083767d74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077565
- Marketing category
- ANDA
- Marketing start
- 2012-03-02
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 60 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 |
|---|
| 71335-9761-1 | 71335976101 | 30 CAPSULE in 1 BOTTLE (71335-9761-1) | 30 capsule | 2023-08-11 | No | No | Historical |
| 71335-9761-2 | 71335976102 | 28 CAPSULE in 1 BOTTLE (71335-9761-2) | 28 capsule | 2023-08-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ziprasidone hydrochloride | Bryant Ranch Prepack | 2023-08-11 | HUMAN PRESCRIPTION DRUG LABEL | 100 |