Imipramine Hydrochloride
- Product NDC
- 0781-1762
- 11-digit product format
- 007811762
- Labeler code
- 0781
- Product ID
- 0781-1762_208bba89-fbc8-4f11-8007-3f8675de8ada
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA084936
- Marketing category
- ANDA
- Marketing start
- 1976-04-20
- 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
- 2022-12-31
- 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 |
|---|
| 0781-1762-01 | 00781176201 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-1762-01) | 1976-04-20 | 0000-00-00 | No | No | Current |
| 0781-1762-10 | 00781176210 | 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1762-10) | 1976-04-20 | 0000-00-00 | No | No | Current |
| 0781-1762-31 | 00781176231 | 30 TABLET, FILM COATED in 1 BOTTLE (0781-1762-31) | 1976-04-20 | 0000-00-00 | No | No | Current |