Nortriptyline Hydrochloride
- Product NDC
- 82804-139
- 11-digit product format
- 828040139
- Labeler code
- 82804
- Product ID
- 82804-139_661ec73c-d893-446a-83c3-218b06889962
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA073556
- Marketing category
- ANDA
- Marketing start
- 2023-11-17
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 25 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 |
|---|
| 82804-139-30 | 82804013930 | 30 CAPSULE in 1 BOTTLE, PLASTIC (82804-139-30) | 30 capsule | 2024-09-06 | No | No | Historical |