Amitriptyline Hydrochloride 00781-1487
Product NDC
00781-1487- Manufacturer
- Sandoz Inc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 21, 1977
- Listing Expires
- December 31, 2026
- Application
- ANDA085968
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amitriptyline Hydrochloride | 25 mg/1 |
Drug Class
Tricyclic Antidepressant [EPC]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (0781-1487-01)
1000 TABLET, FILM COATED in 1 BOTTLE (0781-1487-10)