Tramadol Hydrochloride 00093-3301
Product NDC
00093-3301- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- September 12, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA075977
Active Ingredients
| Ingredient | Strength |
|---|---|
| Tramadol Hydrochloride | 50 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (0093-3301-01)
500 TABLET, FILM COATED in 1 BOTTLE (0093-3301-05)