ziprasidone hydrochloride
- Product NDC
- 63187-168
- 11-digit product format
- 631870168
- Labeler code
- 63187
- Product ID
- 63187-168_67b8d9a0-2da1-4a8d-8775-ecbe065870d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077562
- Marketing category
- ANDA
- Marketing start
- 2013-02-13
- 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 Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-168 | ZIPRASIDONE HYDROCHLORIDE CAPSULE [PROFICIENT RX LP] | 3 | Legacy NDC | 20210121_b650e8b6-6df7-4301-837d-3d3b650b7456.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-168-30 | 63187016830 | 30 CAPSULE in 1 BOTTLE (63187-168-30) | 30 capsule | 2019-01-01 | 0000-00-00 | No | No | Current |
| 63187-168-60 | 63187016860 | 60 CAPSULE in 1 BOTTLE (63187-168-60) | 60 capsule | 2019-01-01 | 0000-00-00 | No | No | Current |