Clomipramine Hydrochloride
- Product NDC
- 70710-1066
- 11-digit product format
- 707101066
- Labeler code
- 70710
- Product ID
- 70710-1066_a988ebbb-6e0c-43ff-83a8-0cc0dc4259ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clomipramine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA208961
- Marketing category
- ANDA
- Marketing start
- 2018-05-03
- Marketing end
- 0000-00-00
- Substance
- CLOMIPRAMINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [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 |
|---|
| 70710-1066-1 | 70710106601 | 100 CAPSULE in 1 BOTTLE (70710-1066-1) | 100 capsule | 2018-05-03 | 0000-00-00 | No | No | Current |
| 70710-1066-3 | 70710106603 | 30 CAPSULE in 1 BOTTLE (70710-1066-3) | 30 capsule | 2018-05-03 | 0000-00-00 | No | No | Current |
| 70710-1066-9 | 70710106609 | 90 CAPSULE in 1 BOTTLE (70710-1066-9) | 90 capsule | 2018-05-03 | 0000-00-00 | No | No | Current |