Imipramine Hydrochloride
- Product NDC
- 42291-347
- 11-digit product format
- 422910347
- Labeler code
- 42291
- Product ID
- 42291-347_d57adc2d-e253-3e2e-e053-2a95a90a3241
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA040903
- Marketing category
- ANDA
- Marketing start
- 2015-12-09
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-347-01 | 42291034701 | 100 TABLET, FILM COATED in 1 BOTTLE (42291-347-01) | 2015-12-09 | 0000-00-00 | No | No | Current |