Desipramine Hydrochloride
- Product NDC
- 71335-0659
- 11-digit product format
- 713350659
- Labeler code
- 71335
- Product ID
- 71335-0659_c462f513-0427-455b-9bfb-f02bdf12a576
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desipramine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208105
- Marketing category
- ANDA
- Marketing start
- 2016-03-21
- Marketing end
- 0000-00-00
- Substance
- DESIPRAMINE 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0659-1 | 71335065901 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0659-1) | 2018-01-29 | 0000-00-00 | No | No | Current |
| 71335-0659-2 | 71335065902 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0659-2) | 2018-01-29 | 0000-00-00 | No | No | Current |
| 71335-0659-3 | 71335065903 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0659-3) | 2018-01-29 | 0000-00-00 | No | No | Current |
| 71335-0659-4 | 71335065904 | 58 TABLET, FILM COATED in 1 BOTTLE (71335-0659-4) | 2018-01-29 | 0000-00-00 | No | No | Current |