ziprasidone hydrochloride
- Product NDC
- 64725-2164
- 11-digit product format
- 647252164
- Labeler code
- 64725
- Product ID
- 64725-2164_85fb1966-59ca-453a-8a7f-17092ef729aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64725-2164-1 | ziprasidone hydrochloride | 30 in 1 CONTAINER | CAPSULE | 30 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-2164 | ZIPRASIDONE HYDROCHLORIDE CAPSULE [TYA PHARMACEUTICALS] | 4 | Legacy NDC, 1 package rows | 20140921_5752ef72-c515-4ead-a359-69d4761ad7f4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-2164-1 | 64725216401 | 30 in 1 CONTAINER | Historical |