ziprasidone hydrochloride
- Product NDC
- 71335-0263
- 11-digit product format
- 713350263
- Labeler code
- 71335
- Product ID
- 71335-0263_ab55f686-1af5-4ba1-9e59-faf674a8dd7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077562
- Marketing category
- ANDA
- Marketing start
- 2013-02-13
- Marketing end
- 0000-00-00
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 80 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0263-1 | 71335026301 | 60 CAPSULE in 1 BOTTLE (71335-0263-1) | 60 capsule | 2017-02-13 | 0000-00-00 | No | No | Current |
| 71335-0263-2 | 71335026302 | 30 CAPSULE in 1 BOTTLE (71335-0263-2) | 30 capsule | 2017-02-13 | 0000-00-00 | No | No | Current |
| 71335-0263-3 | 71335026303 | 28 CAPSULE in 1 BOTTLE (71335-0263-3) | 28 capsule | 2017-02-13 | 0000-00-00 | No | No | Current |
| 71335-0263-4 | 71335026304 | 90 CAPSULE in 1 BOTTLE (71335-0263-4) | 90 capsule | 2021-12-27 | 0000-00-00 | No | No | Current |