DESIPRAMINE HYDROCHLORIDE
- Product NDC
- 72189-104
- 11-digit product format
- 721890104
- Labeler code
- 72189
- Product ID
- 72189-104_a7e6d256-7227-3334-e053-2995a90aa96d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DESIPRAMINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA072099
- Marketing category
- ANDA
- Marketing start
- 2020-06-12
- Marketing end
- 0000-00-00
- Substance
- DESIPRAMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-104-30 | DESIPRAMINE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-104 | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [DIRECT RX] | 1 | Legacy NDC, 1 package rows | 20200613_a7e6d256-7226-3334-e053-2995a90aa96d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-104-30 | 72189010430 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-104-30) | 2020-06-12 | 0000-00-00 | No | No | Current |