DESIPRAMINE HYDROCHLORIDE
- Product NDC
- 70518-4645
- 11-digit product format
- 705184645
- Labeler code
- 70518
- Product ID
- 70518-4645_508a8ae7-c52d-9157-e063-6294a90a2c9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desipramine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204963
- Marketing category
- ANDA
- Marketing start
- 2026-04-28
- Substance
- DESIPRAMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DESIPRAMINE HYDROCHLORIDE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DESIPRAMINE HYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1Y58DO4MY1 |
| Rxcui | 1099288 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4645-0 | DESIPRAMINE HYDROCHLORIDE | 50 in 1 BOX | TABLET | 50 | | 1 |
| 70518-4645-1 | DESIPRAMINE HYDROCHLORIDE | 1 in 1 POUCH | TABLET | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4645-0 | 70518464500 | 50 POUCH in 1 BOX (70518-4645-0) / 1 TABLET in 1 POUCH (70518-4645-1) | 50 pouch | 2026-04-28 | No | No | Historical |
| 70518-4645-1 | 70518464501 | 1 in 1 POUCH | | | | | Historical |