Ziprasidone Hydrochloride
- Product NDC
- 70518-2940
- 11-digit product format
- 705182940
- Labeler code
- 70518
- Product ID
- 70518-2940_e930d485-7270-c042-e053-2995a90a6fdf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204117
- Marketing category
- ANDA
- Marketing start
- 2020-11-13
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-2940-0 | 70518294000 | 30 CAPSULE in 1 BLISTER PACK (70518-2940-0) | 30 capsule | 2020-11-13 | 0000-00-00 | No | No | Current |
| 70518-2940-1 | 70518294001 | 30 POUCH in 1 BOX (70518-2940-1) > 1 CAPSULE in 1 POUCH (70518-2940-2) | 30 pouch | 2021-02-08 | 0000-00-00 | No | No | Current |