Desipramine Hydrochloride
- Product NDC
- 62135-595
- 11-digit product format
- 621350595
- Labeler code
- 62135
- Product ID
- 62135-595_45895d97-14b1-1beb-e063-6394a90a2930
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desipramine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA207433
- Marketing category
- ANDA
- Marketing start
- 2016-11-01
- Substance
- DESIPRAMINE HYDROCHLORIDE
- Active strength
- 50 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 | 50 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 |
|---|
| 62135-595-12 | Desipramine Hydrochloride | 120 in 1 BOTTLE | TABLET | 120 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-595 | DESIPRAMINE HYDROCHLORIDE TABLET [CHARTWELL RX, LLC] | 2 | Current NDC, 1 package rows | 20241011_6ab5e113-82ef-493d-a4e3-a2756608fa60.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-595-12 | 62135059512 | 120 TABLET in 1 BOTTLE (62135-595-12) | 120 tablet | 2023-05-12 | No | No | Historical |