Ziprasidone Hydrochloride
- Product NDC
- 70518-3048
- 11-digit product format
- 705183048
- Labeler code
- 70518
- Product ID
- 70518-3048_bdbbf09b-2aee-6ec9-e053-2995a90afdc1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204117
- Marketing category
- ANDA
- Marketing start
- 2021-03-16
- 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
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 |
|---|
| 70518-3048-0 | 70518304800 | 30 POUCH in 1 BOX (70518-3048-0) > 1 CAPSULE in 1 POUCH (70518-3048-1) | 30 pouch | 2021-03-16 | 0000-00-00 | No | No | Current |