Imipramine Hydrochloride
- Product NDC
- 49884-055
- 11-digit product format
- 498840055
- Labeler code
- 49884
- Product ID
- 49884-055_2e41fb61-bc65-4d6e-99a9-e710d3f12d8c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA088262
- Marketing category
- ANDA
- Marketing start
- 1983-10-21
- 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 |
|---|
| 49884-055-01 | 49884005501 | 100 TABLET in 1 BOTTLE (49884-055-01) | 100 tablet | 1983-11-01 | 0000-00-00 | No | No | Current |
| 49884-055-10 | 49884005510 | 1000 TABLET in 1 BOTTLE (49884-055-10) | 1000 tablet | 1983-11-01 | 0000-00-00 | No | No | Current |