Doxepin Hydrochloride 51672-4247
Product NDC
51672-4247- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 7, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA219058
Need to source Doxepin Hydrochloride? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Doxepin Hydrochloride | 6 mg/1 |
Drug Class
Tricyclic Antidepressant [EPC]
Packaging Options(1)
30 TABLET in 1 BOTTLE (51672-4247-2)