Clomipramine Hydrochloride
- Product NDC
- 0781-2037
- 11-digit product format
- 007812037
- Labeler code
- 0781
- Product ID
- 0781-2037_2438e626-5cd3-4bd6-b53f-172bc305dd37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clomipramine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA074364
- Marketing category
- ANDA
- Marketing start
- 1996-03-29
- 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
- 2021-12-31
- 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 |
|---|
| 0781-2037-01 | 00781203701 | 100 CAPSULE in 1 BOTTLE (0781-2037-01) | 100 capsule | 1996-03-29 | 0000-00-00 | No | No | Current |