ziprasidone hydrochloride
- Product NDC
- 63629-7104
- 11-digit product format
- 636297104
- Labeler code
- 63629
- Product ID
- 63629-7104_e85cb454-42c4-4da7-8cab-78f7aa32e067
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone HCl
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077561
- Marketing category
- ANDA
- Marketing start
- 2012-05-14
- Marketing end
- 0000-00-00
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-7104-1 | 63629710401 | 30 CAPSULE in 1 BOTTLE (63629-7104-1) | 30 capsule | 2016-09-29 | 0000-00-00 | No | No | Current |
| 63629-7104-2 | 63629710402 | 28 CAPSULE in 1 BOTTLE (63629-7104-2) | 28 capsule | 2016-09-29 | 0000-00-00 | No | No | Current |