Ziprasidone Hydrochloride
- Product NDC
- 50090-5785
- 11-digit product format
- 500905785
- Labeler code
- 50090
- Product ID
- 50090-5785_8e8669be-14ef-4b48-8304-a1b03ec26dd0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204375
- Marketing category
- ANDA
- Marketing start
- 2017-02-18
- 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5785-0 | Ziprasidone Hydrochloride | 1 in 1 CARTON | CAPSULE | 1 | | 1 |
| 50090-5785-0 | Ziprasidone Hydrochloride | 40 in 1 BOX, UNIT-DOSE | CAPSULE | 40 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5785 | ZIPRASIDONE HYDROCHLORIDE CAPSULE [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20211020_0d1b00e8-0a71-493c-808f-bd1ec945842b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5785-0 | 50090578500 | 1 BOX, UNIT-DOSE in 1 CARTON (50090-5785-0) > 40 CAPSULE in 1 BOX, UNIT-DOSE | 2021-10-08 | 0000-00-00 | No | No | Current |