DESIPRAMINE HYDROCHLORIDE
- Product NDC
- 50742-117
- 11-digit product format
- 507420117
- Labeler code
- 50742
- Product ID
- 50742-117_7a0e5dd9-7456-4774-b529-ce9d5627b654
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desipramine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA204963
- Marketing category
- ANDA
- Marketing start
- 2018-09-19
- Substance
- DESIPRAMINE HYDROCHLORIDE
- Active strength
- 150 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
- DESIPRAMINE HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DESIPRAMINE HYDROCHLORIDE | 150 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1Y58DO4MY1 |
| Rxcui | 1099288, 1099292, 1099296, 1099300, 1099304, 1099316 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50742-117-50 | DESIPRAMINE HYDROCHLORIDE | 50 in 1 BOTTLE | TABLET | 50 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50742-117 | DESIPRAMINE HYDROCHLORIDE TABLET [INGENUS PHARMACEUTICALS, LLC] | 11 | Current NDC, Legacy NDC, 1 package rows | 20230627_7280f157-3fff-41c5-b3f4-510b8bacdaba.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-117-50 | 50742011750 | 50 TABLET in 1 BOTTLE (50742-117-50) | 50 tablet | 2018-09-19 | 0000-00-00 | No | No | Current |