Imipramine Hydrochloride
- Product NDC
- 55700-710
- 11-digit product format
- 557000710
- Labeler code
- 55700
- Product ID
- 55700-710_433ca886-a1e1-45e8-9810-c66d0aa4b935
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA040903
- Marketing category
- ANDA
- Marketing start
- 2018-12-14
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-710-30 | 55700071030 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-710-30) | 2018-12-14 | 0000-00-00 | No | No | Current |