Tramadol Hydrochloride 80425-0548
Product NDC
80425-0548- Manufacturer
- Advanced Rx Of Tennessee, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- August 27, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA211825
Active Ingredients
| Ingredient | Strength |
|---|---|
| Tramadol Hydrochloride | 50 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(8)
15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-1)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-2)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-3)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-4)
120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-5)
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-6)
180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-7)
240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-8)