Ziprasidone hydrochloride
- Product NDC
- 64679-993
- 11-digit product format
- 646790993
- Labeler code
- 64679
- Product ID
- 64679-993_83bb92ad-8d72-4b8d-958a-ff4c97c9c2ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ziprasidone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA090348
- Marketing category
- ANDA
- Marketing start
- 2012-09-01
- Marketing end
- 0000-00-00
- Substance
- ZIPRASIDONE HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
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 |
|---|
| 64679-993-01 | 64679099301 | 30 CAPSULE in 1 BOTTLE (64679-993-01) | 30 capsule | 2012-09-01 | 0000-00-00 | No | No | Current |
| 64679-993-02 | 64679099302 | 60 CAPSULE in 1 BOTTLE (64679-993-02) | 60 capsule | 2012-09-01 | 0000-00-00 | No | No | Current |
| 64679-993-03 | 64679099303 | 100 CAPSULE in 1 BOTTLE (64679-993-03) | 100 capsule | 2012-09-01 | 0000-00-00 | No | No | Current |
| 64679-993-04 | 64679099304 | 500 CAPSULE in 1 BOTTLE (64679-993-04) | 500 capsule | 2012-09-01 | 0000-00-00 | No | No | Current |
| 64679-993-06 | 64679099306 | 10 BLISTER PACK in 1 CARTON (64679-993-06) > 8 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2012-09-01 | 0000-00-00 | No | No | Current |