Nortriptyline Hydrochloride
- Product NDC
- 67046-1500
- 11-digit product format
- 670461500
- Labeler code
- 67046
- Product ID
- 67046-1500_2ccb449d-506d-2098-e063-6394a90a74c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA073556
- Marketing category
- ANDA
- Marketing start
- 2025-01-28
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 67046-1500-3 | 67046150003 | 30 CAPSULE in 1 BLISTER PACK (67046-1500-3) | 30 capsule | 2025-01-28 | No | No | Historical |