Nortriptyline Hydrochloride
- Product NDC
- 60687-911
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA074132
- Marketing category
- ANDA
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 60687-911-01 | 100 BLISTER PACK in 1 CARTON (60687-911-01) / 1 CAPSULE in 1 BLISTER PACK (60687-911-11) | 2025-12-01 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Nortriptyline Hydrochloride Capsules, USP Rx Only 8490001/0425F | American Health Packaging | 2025-12-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |