Tramadol Hydrochloride 27808-0301
Product NDC
27808-0301- Manufacturer
- Cranbury Pharmaceuticals, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- December 22, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA091498
Active Ingredients
| Ingredient | Strength |
|---|---|
| Tramadol Hydrochloride | 50 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (27808-301-01)
500 TABLET, FILM COATED in 1 BOTTLE (27808-301-02)
1000 TABLET, FILM COATED in 1 BOTTLE (27808-301-03)