Tramadol Hydrochloride 68788-4035
Product NDC
68788-4035- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- September 29, 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(9)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-1)
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-2)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-3)
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-4)
15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-5)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-6)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-7)
120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-8)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-9)