Nortriptyline Hydrochloride
- Product NDC
- 72789-425
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA073556
- Marketing category
- ANDA
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 72789-425-30 | 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-425-30) | 2024-08-07 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Nortriptyline Hydrochloride Capsules, USP | PD-Rx Pharmaceuticals, Inc. | 2025-10-14 | HUMAN PRESCRIPTION DRUG LABEL | 3 |
| Nortriptyline Hydrochloride Capsules, USP | PD-Rx Pharmaceuticals, Inc. | 2024-08-07 | HUMAN PRESCRIPTION DRUG LABEL | 2 |