Ziprasidone Hydrochloride
- Product NDC
- 71335-0729
- 11-digit product format
- 713350729
- Labeler code
- 71335
- Product ID
- 71335-0729_7e8cb689-eba3-43e0-9e66-dcae27c8ba3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204117
- Marketing category
- ANDA
- Marketing start
- 2016-12-27
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0729-1 | 71335072901 | 60 CAPSULE in 1 BOTTLE (71335-0729-1) | 60 capsule | 2018-03-12 | 0000-00-00 | No | No | Current |
| 71335-0729-2 | 71335072902 | 30 CAPSULE in 1 BOTTLE (71335-0729-2) | 30 capsule | 2018-04-19 | 0000-00-00 | No | No | Current |
| 71335-0729-3 | 71335072903 | 28 CAPSULE in 1 BOTTLE (71335-0729-3) | 28 capsule | 2022-03-09 | 0000-00-00 | No | No | Current |
| 71335-0729-4 | 71335072904 | 90 CAPSULE in 1 BOTTLE (71335-0729-4) | 90 capsule | 2022-03-09 | 0000-00-00 | No | No | Current |