Imipramine Hydrochloride
- Product NDC
- 63629-8149
- 11-digit product format
- 636298149
- Labeler code
- 63629
- Product ID
- 63629-8149_7d11d2e3-d513-42a0-99f0-3ddf8abe459d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA088292
- Marketing category
- ANDA
- Marketing start
- 1983-10-21
- Marketing end
- 0000-00-00
- Substance
- IMIPRAMINE HYDROCHLORIDE
- Active strength
- 10 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8149-1 | 63629814901 | 30 TABLET in 1 BOTTLE (63629-8149-1) | 30 tablet | 2019-06-11 | 0000-00-00 | No | No | Current |