Ziprasidone Hydrochloride
- Product NDC
- 68001-137
- 11-digit product format
- 680010137
- Labeler code
- 68001
- Product ID
- 68001-137_c4f8ca78-8588-7b86-e053-2995a90aaaa9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA077560
- Marketing category
- ANDA
- Marketing start
- 2014-02-26
- Marketing end
- 2021-09-30
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68001-137-06 | 68001013706 | 60 CAPSULE in 1 BOTTLE (68001-137-06) | 60 capsule | 2014-02-26 | 2021-09-30 | No | No | Current |