Imipramine Hydrochloride
- Product NDC
- 50090-0034
- 11-digit product format
- 500900034
- Labeler code
- 50090
- Product ID
- 50090-0034_72b9a3d9-9253-4833-88fd-1e49a7873e81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#