Desipramine Hydrochloride
- Product NDC
- 71335-0208
- 11-digit product format
- 713350208
- Labeler code
- 71335
- Product ID
- 71335-0208_731e919e-9c0b-4693-b462-b1712a413fe2
- 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
- 100 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 |
|---|
| 71335-0208-1 | 71335020801 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0208-1) | 2022-02-09 | 0000-00-00 | No | No | Current |
| 71335-0208-2 | 71335020802 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0208-2) | 2022-02-09 | 0000-00-00 | No | No | Current |
| 71335-0208-3 | 71335020803 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0208-3) | 2022-02-09 | 0000-00-00 | No | No | Current |
| 71335-0208-4 | 71335020804 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0208-4) | 2022-02-09 | 0000-00-00 | No | No | Current |
| 71335-0208-5 | 71335020805 | 8 TABLET, FILM COATED in 1 BOTTLE (71335-0208-5) | 2022-02-09 | 0000-00-00 | No | No | Current |