Desipramine Hydrochloride
- Product NDC
- 63629-7596
- 11-digit product format
- 636297596
- Labeler code
- 63629
- Product ID
- 63629-7596_89b0438b-9701-4c1b-9e8a-f0a32c3af916
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074430
- Marketing category
- ANDA
- Marketing start
- 2006-05-09
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7596-1 | 63629759601 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7596-1) | 2018-05-09 | 0000-00-00 | No | No | Current |