ziprasidone hydrochloride
- Product NDC
- 50090-3823
- 11-digit product format
- 500903823
- Labeler code
- 50090
- Product ID
- 50090-3823_8e3bf6a7-1916-4cf0-83a1-137f37b858e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077562
- Marketing category
- ANDA
- Marketing start
- 2013-02-13
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3823-0 | ziprasidone hydrochloride | 40 in 1 BOTTLE | CAPSULE | 40 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3823 | ZIPRASIDONE HYDROCHLORIDE CAPSULE [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 1 package rows | 20211104_0721cc7e-9560-4ca4-95e1-5c3a4d32c572.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3823-0 | 50090382300 | 40 CAPSULE in 1 BOTTLE (50090-3823-0) | 40 capsule | 2018-11-13 | 0000-00-00 | No | No | Current |