DESIPRAMINE HYDROCHLORIDE
- Product NDC
- 23155-583
- 11-digit product format
- 231550583
- Labeler code
- 23155
- Product ID
- 23155-583_46db00eb-aab8-4795-ac06-1de3f46268f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desipramine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA207433
- Marketing category
- ANDA
- Marketing start
- 2016-11-01
- Marketing end
- 0000-00-00
- Substance
- DESIPRAMINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 23155-583-25 | DESIPRAMINE HYDROCHLORIDE | 50 in 1 BOTTLE | TABLET | 50 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 23155-583 | DESIPRAMINE HYDROCHLORIDE TABLET [HERITAGE PHARMACEUTICALS INC. D/B/A AVET PHARMACEUTICALS INC.] | 7 | Legacy NDC, 1 package rows | 20230823_ee14dd2c-c54b-4cd1-a3a0-f7ad5a5a0ed0.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 |
|---|
| 23155-583-25 | 23155058325 | 50 TABLET in 1 BOTTLE (23155-583-25) | 50 tablet | 2016-11-01 | 0000-00-00 | No | No | Current |