Imipramine Hydrochloride
- Product NDC
- 70518-1793
- 11-digit product format
- 705181793
- Labeler code
- 70518
- Product ID
- 70518-1793_d6866e4e-c5ec-7b9b-e053-2995a90a6309
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA088262
- Marketing category
- ANDA
- Marketing start
- 2019-01-11
- Marketing end
- 0000-00-00
- Substance
- IMIPRAMINE HYDROCHLORIDE
- Active strength
- 25 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 |
|---|
| 70518-1793-0 | 70518179300 | 30 TABLET in 1 BLISTER PACK (70518-1793-0) | 30 tablet | 2019-01-11 | 0000-00-00 | No | No | Current |
| 70518-1793-1 | 70518179301 | 30 TABLET in 1 BLISTER PACK (70518-1793-1) | 30 tablet | 2020-12-18 | 0000-00-00 | No | No | Current |