Amitriptyline Hydrochloride 57664-0691
Product NDC
57664-0691- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 14, 1987
- Listing Expires
- December 31, 2026
- Application
- ANDA089399
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amitriptyline Hydrochloride | 150 mg/1 |
Drug Class
Tricyclic Antidepressant [EPC]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-691-88)