Ziprasidone Hydrochloride
- Product NDC
- 68001-450
- 11-digit product format
- 680010450
- Labeler code
- 68001
- Product ID
- 68001-450_326cdd3c-c314-ff98-e063-6294a90a2a20
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA204117
- Marketing category
- ANDA
- Marketing start
- 2020-08-31
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ziprasidone Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZIPRASIDONE HYDROCHLORIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 216X081ORU |
| Rxcui | 313776, 313777, 313778, 314286 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68001-450-06 | Ziprasidone Hydrochloride | 60 in 1 BOTTLE | CAPSULE | 60 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68001-450 | ZIPRASIDONE HYDROCHLORIDE CAPSULE [BLUEPOINT LABORATORIES] | 8 | Current NDC, Legacy NDC, 1 package rows | 20250417_c0eb7b4d-0264-4eed-8756-51bba3af82fb.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 |
|---|
| 68001-450-06 | 68001045006 | 60 CAPSULE in 1 BOTTLE (68001-450-06) | 60 capsule | 2020-08-31 | 0000-00-00 | No | No | Current |