Ziprasidone Hydrochloride
- Product NDC
- 70518-0757
- 11-digit product format
- 705180757
- Labeler code
- 70518
- Product ID
- 70518-0757_ecfc0323-775c-58cc-e053-2a95a90a6c54
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204375
- Marketing category
- ANDA
- Marketing start
- 2017-10-04
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0757 | ZIPRASIDONE HYDROCHLORIDE CAPSULE [REMEDYREPACK INC.] | 13 | Legacy NDC | 20250429_d858c3ef-696c-4eb0-9afc-15ba4d741746.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0757-0 | 70518075700 | 30 CAPSULE in 1 BLISTER PACK (70518-0757-0) | 30 capsule | 2017-10-04 | 0000-00-00 | No | No | Current |
| 70518-0757-1 | 70518075701 | 30 POUCH in 1 BOX (70518-0757-1) > 1 CAPSULE in 1 POUCH (70518-0757-2) | 30 pouch | 2021-11-24 | 0000-00-00 | No | No | Current |