Clozapine
- Product NDC
- 0093-7772
- 11-digit product format
- 000937772
- Labeler code
- 0093
- Product ID
- 0093-7772_46cf5a5f-6610-4c5d-bac8-b9219fa9b699
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clozapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA074949
- Marketing category
- ANDA
- Marketing start
- 2009-09-18
- Marketing end
- 0000-00-00
- Substance
- CLOZAPINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-7772-01 | 00093777201 | 100 TABLET in 1 BOTTLE (0093-7772-01) | 100 tablet | 2009-09-18 | 0000-00-00 | No | No | Current |
| 0093-7772-05 | 00093777205 | 500 TABLET in 1 BOTTLE (0093-7772-05) | 500 tablet | 2009-09-18 | 0000-00-00 | No | No | Current |
| 0093-7772-93 | 00093777293 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0093-7772-93) > 1 TABLET in 1 BLISTER PACK (0093-7772-19) | 100 blister pack | 2010-04-12 | 0000-00-00 | No | No | Current |