Desipramine Hydrochloride
- Product NDC
- 68788-7552
- 11-digit product format
- 687887552
- Labeler code
- 68788
- Product ID
- 68788-7552_ff6c9877-6178-42ff-9e1e-1ac18eb1f277
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA205153
- Marketing category
- ANDA
- Marketing start
- 2019-01-22
- 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 |
|---|
| 68788-7552-1 | 68788755201 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7552-1) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7552-3 | 68788755203 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7552-3) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7552-6 | 68788755206 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7552-6) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7552-9 | 68788755209 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7552-9) | 2019-12-27 | 0000-00-00 | No | No | Current |