Imipramine Hydrochloride
- Product NDC
- 71335-2601
- 11-digit product format
- 713352601
- Labeler code
- 71335
- Product ID
- 71335-2601_47b2a18c-4497-42e0-a2fe-8e8f2761400e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040903
- Marketing category
- ANDA
- Marketing start
- 2016-04-07
- Substance
- IMIPRAMINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| BKE5Q1J60U | IMIPRAMINE HYDROCHLORIDE | 113-52-0 | IMIPRAMINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2601-1 | 71335260101 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2601-1) | 2025-06-05 | No | No | Historical |
| 71335-2601-2 | 71335260102 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2601-2) | 2025-06-05 | No | No | Historical |
| 71335-2601-3 | 71335260103 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2601-3) | 2025-06-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Imipramine Hydrochloride | Bryant Ranch Prepack | 2025-06-05 | HUMAN PRESCRIPTION DRUG LABEL | 1 |