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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Imipramine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IMIPRAMINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | BKE5Q1J60U |
| Rxcui | 835564 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2601-1 | Imipramine Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
| 71335-2601-2 | Imipramine Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
| 71335-2601-3 | Imipramine Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |
| 71335-2601-2 | 71335260102 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2601-2) | 2025-06-05 | No | No | Current |
| 71335-2601-3 | 71335260103 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2601-3) | 2025-06-05 | No | No | Current |