Nortriptyline HCL
- Product NDC
- 61919-853
- 11-digit product format
- 619190853
- Labeler code
- 61919
- Product ID
- 61919-853_db70b191-976f-789e-e053-2995a90a1b0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline HCL
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2019-06-04
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 00FN6IH15D | NORTRIPTYLINE HYDROCHLORIDE | 894-71-3 | NORTRIPTYLINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-853-30 | 61919085330 | 30 CAPSULE in 1 BOTTLE (61919-853-30) | 30 capsule | 2019-06-04 | 0000-00-00 | No | No | Current |
| 61919-853-90 | 61919085390 | 90 CAPSULE in 1 BOTTLE (61919-853-90) | 90 capsule | 2019-06-04 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| NORTRIPTYLINE HCL | Direct_Rx | 2022-03-30 | HUMAN PRESCRIPTION DRUG LABEL | 2 |