Imipramine Hydrochloride
- Product NDC
- 68071-2730
- 11-digit product format
- 680712730
- Labeler code
- 68071
- Product ID
- 68071-2730_dfb479a9-d6da-d36d-e053-2a95a90ae4f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA088276
- Marketing category
- ANDA
- Marketing start
- 1983-10-21
- Marketing end
- 0000-00-00
- Substance
- IMIPRAMINE HYDROCHLORIDE
- Active strength
- 50 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 |
|---|
| 68071-2730-9 | 68071273009 | 90 TABLET in 1 BOTTLE (68071-2730-9) | 90 tablet | 2022-05-23 | 0000-00-00 | No | No | Current |