Nortriptyline Hydrochloride
- Product NDC
- 71335-1552
- 11-digit product format
- 713351552
- Labeler code
- 71335
- Product ID
- 71335-1552_1c7ab195-2d22-4021-9af0-f77317695c7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2000-05-08
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 71335-1552-1 | 71335155201 | 30 CAPSULE in 1 BOTTLE (71335-1552-1) | 30 capsule | 2020-03-31 | No | No | Historical |
| 71335-1552-2 | 71335155202 | 60 CAPSULE in 1 BOTTLE (71335-1552-2) | 60 capsule | 2020-03-31 | No | No | Historical |
| 71335-1552-3 | 71335155203 | 90 CAPSULE in 1 BOTTLE (71335-1552-3) | 90 capsule | 2020-03-31 | No | No | Historical |
| 71335-1552-4 | 71335155204 | 28 CAPSULE in 1 BOTTLE (71335-1552-4) | 28 capsule | 2020-03-31 | No | No | Historical |