Ziprasidone Hydrochloride
- Product NDC
- 70518-2757
- 11-digit product format
- 705182757
- Labeler code
- 70518
- Product ID
- 70518-2757_d6e82ca2-aace-b844-e053-2a95a90a07b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204117
- Marketing category
- ANDA
- Marketing start
- 2020-05-27
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 216X081ORU | ZIPRASIDONE HYDROCHLORIDE | 138982-67-9 | ZIPRASIDONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2757-0 | 70518275700 | 30 CAPSULE in 1 BLISTER PACK (70518-2757-0) | 30 capsule | 2020-05-27 | 0000-00-00 | No | No | Current |