ziprasidone hydrochloride
- Product NDC
- 70518-1586
- 11-digit product format
- 705181586
- Labeler code
- 70518
- Product ID
- 70518-1586_d35a6b43-4fe6-342e-e053-2995a90a30db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077562
- Marketing category
- ANDA
- Marketing start
- 2018-10-24
- 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
- 2022-12-31
- 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 |
|---|
| 70518-1586 | ZIPRASIDONE HYDROCHLORIDE CAPSULE [REMEDYREPACK INC.] | 13 | Legacy NDC | 20250226_61e3fa7b-61c2-4d5d-a6b3-2618c15a6bd9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1586-0 | 70518158600 | 30 CAPSULE in 1 BLISTER PACK (70518-1586-0) | 30 capsule | 2018-10-24 | 0000-00-00 | No | No | Current |
| 70518-1586-1 | 70518158601 | 30 POUCH in 1 BOX, UNIT-DOSE (70518-1586-1) > 1 CAPSULE in 1 POUCH (70518-1586-2) | 30 pouch | 2019-10-21 | 0000-00-00 | No | No | Current |