Desipramine Hydrochloride
- Product NDC
- 71335-0941
- 11-digit product format
- 713350941
- Labeler code
- 71335
- Product ID
- 71335-0941_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
- 10 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 |
|---|
| 71335-0941-1 | 71335094101 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0941-1) | 2018-08-30 | 0000-00-00 | No | No | Current |