Desipramine Hydrochloride
- Product NDC
- 68788-7750
- 11-digit product format
- 687887750
- Labeler code
- 68788
- Product ID
- 68788-7750_7a7dcea4-b23d-4c31-9c64-69f9a42bfe7e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA072101
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- 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
- 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 |
|---|
| 68788-7750-1 | 68788775001 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7750-1) | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7750-3 | 68788775003 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7750-3) | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7750-6 | 68788775006 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7750-6) | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7750-9 | 68788775009 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7750-9) | 2020-07-01 | 0000-00-00 | No | No | Current |