Nortriptyline Hydrochloride
- Product NDC
- 70771-1614
- 11-digit product format
- 707711614
- Labeler code
- 70771
- Product ID
- 70771-1614_b2965133-3b71-4cdb-8676-235882e57beb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA213441
- Marketing category
- ANDA
- Marketing start
- 2022-02-10
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 50 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 |
|---|
| 70771-1614-1 | 70771161401 | 100 CAPSULE in 1 BOTTLE (70771-1614-1) | 100 capsule | 2022-02-10 | No | No | Historical |
| 70771-1614-3 | 70771161403 | 30 CAPSULE in 1 BOTTLE (70771-1614-3) | 30 capsule | 2022-02-10 | No | No | Historical |
| 70771-1614-5 | 70771161405 | 500 CAPSULE in 1 BOTTLE (70771-1614-5) | 500 capsule | 2022-02-10 | No | No | Historical |