ziprasidone hydrochloride
- Product NDC
- 63739-005
- 11-digit product format
- 637390005
- Labeler code
- 63739
- Product ID
- 63739-005_dae92d33-fd35-5411-e053-2a95a90ad330
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA077565
- Marketing category
- ANDA
- Marketing start
- 2012-03-02
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-005 | ZIPRASIDONE HYDROCHLORIDE CAPSULE [MCKESSON CORPORATION DBA SKY PACKAGING] | 16 | Legacy NDC | 20250119_db621e08-aa2a-43b9-9d6e-33a633c0f648.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-005-32 | 63739000532 | 4 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-005-32) > 10 CAPSULE in 1 BLISTER PACK | 4 blister pack | 2016-01-11 | 0000-00-00 | No | No | Current |