Ziprasidone
- Product NDC
- 70771-1182
- 11-digit product format
- 707711182
- Labeler code
- 70771
- Product ID
- 70771-1182_58405edd-2565-4bbb-80fa-5b3cb9ff6f4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA208988
- Marketing category
- ANDA
- Marketing start
- 2017-12-28
- Marketing end
- 0000-00-00
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 40 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 |
|---|
| 70771-1182 | ZIPRASIDONE CAPSULE [ZYDUS LIFESCIENCES LIMITED] | 5 | Legacy NDC | 20231005_d607e3c2-62f5-4f4c-bbb3-423ac9478420.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1182-5 | 70771118205 | 500 CAPSULE in 1 BOTTLE (70771-1182-5) | 500 capsule | 2017-12-28 | 0000-00-00 | No | No | Current |
| 70771-1182-6 | 70771118206 | 60 CAPSULE in 1 BOTTLE (70771-1182-6) | 60 capsule | 2017-12-28 | 0000-00-00 | No | No | Current |
| 70771-1182-8 | 70771118208 | 8 BLISTER PACK in 1 CARTON (70771-1182-8) > 10 CAPSULE in 1 BLISTER PACK (70771-1182-2) | 8 blister pack | 2017-12-28 | 0000-00-00 | No | No | Current |