ziprasidone hydrochloride
- Product NDC
- 50090-4821
- 11-digit product format
- 500904821
- Labeler code
- 50090
- Product ID
- 50090-4821_a16c9264-87ca-414d-a504-ba0a85334b77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077565
- Marketing category
- ANDA
- Marketing start
- 2018-07-26
- Marketing end
- 0000-00-00
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-4821-0 | 50090482100 | 40 CAPSULE in 1 BOTTLE (50090-4821-0) | 40 capsule | 2019-12-31 | 0000-00-00 | No | No | Current |