Imipramine Hydrochloride
- Product NDC
- 60429-095
- 11-digit product format
- 604290095
- Labeler code
- 60429
- Product ID
- 60429-095_dc6778bb-d0f4-be8c-e053-2995a90a1e12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-095-01 | 60429009501 | 100 TABLET in 1 BOTTLE (60429-095-01) | 100 tablet | 1999-08-27 | 0000-00-00 | No | No | Current |