ziprasidone hydrochloride
- Product NDC
- 70518-2366
- 11-digit product format
- 705182366
- Labeler code
- 70518
- Product ID
- 70518-2366_c895d928-7677-80ea-e053-2995a90aa2c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077562
- Marketing category
- ANDA
- Marketing start
- 2019-10-17
- 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
- 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 |
|---|
| 70518-2366-0 | 70518236600 | 30 POUCH in 1 BOX, UNIT-DOSE (70518-2366-0) > 1 CAPSULE in 1 POUCH (70518-2366-1) | 30 pouch | 2019-10-17 | 0000-00-00 | No | No | Current |