Ziprasidone hydrochloride
- Product NDC
- 64725-0994
- 11-digit product format
- 647250994
- Labeler code
- 64725
- Product ID
- 64725-0994_3661200b-ba45-45c7-b29b-714b1fe94955
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA090348
- Marketing category
- ANDA
- Marketing start
- 2012-09-01
- Marketing end
- 0000-00-00
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 80 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 |
|---|
| 64725-0994-1 | Ziprasidone hydrochloride | 60 in 1 BOTTLE | CAPSULE | 60 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-0994 | ZIPRASIDONE HYDROCHLORIDE CAPSULE [TYA PHARMACEUTICALS] | 4 | Legacy NDC, 1 package rows | 20141031_4890cf77-8da3-46ae-b6f6-abea7aae6b4d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-0994-1 | 64725099401 | 60 in 1 BOTTLE | Historical |