Desipramine Hydrochloride
- Product NDC
- 0781-8976
- 11-digit product format
- 007818976
- Labeler code
- 0781
- Product ID
- 0781-8976_83ae3fcf-2c05-4ee1-8e68-6649eda49344
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA072104
- Marketing category
- ANDA
- Marketing start
- 1988-06-20
- Marketing end
- 0000-00-00
- Substance
- DESIPRAMINE HYDROCHLORIDE
- Active strength
- 150 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-8976-50 | 00781897650 | 50 TABLET, FILM COATED in 1 BOTTLE (0781-8976-50) | 2018-06-27 | 0000-00-00 | No | No | Current |