Ziprasidone
- Product NDC
- 72578-023
- 11-digit product format
- 725780023
- Labeler code
- 72578
- Product ID
- 72578-023_4e34da24-9048-483e-9241-eb1c036bf6ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Viona Pharmaceuticals Inc
- Application
- ANDA208988
- Marketing category
- ANDA
- Marketing start
- 2020-09-15
- 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
- 2021-12-31
- 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 |
|---|
| 72578-023-05 | 72578002305 | 500 CAPSULE in 1 BOTTLE (72578-023-05) | 500 capsule | 2020-09-15 | 0000-00-00 | No | No | Current |
| 72578-023-14 | 72578002314 | 60 CAPSULE in 1 BOTTLE (72578-023-14) | 60 capsule | 2020-09-15 | 0000-00-00 | No | No | Current |
| 72578-023-80 | 72578002380 | 8 BLISTER PACK in 1 CARTON (72578-023-80) > 10 CAPSULE in 1 BLISTER PACK | 8 blister pack | 2020-09-15 | 0000-00-00 | No | No | Current |