Tramadol Hydrochloride And Acetaminophen 65862-0922
Product NDC
65862-0922- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- March 22, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA207152
Active Ingredients
| Ingredient | Strength |
|---|---|
| Acetaminophen | 325 mg/1 |
| Tramadol Hydrochloride | 37.5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(5)
100 TABLET, FILM COATED in 1 BOTTLE (65862-922-01)
500 TABLET, FILM COATED in 1 BOTTLE (65862-922-05)
30 TABLET, FILM COATED in 1 BOTTLE (65862-922-30)
10 BLISTER PACK in 1 CARTON (65862-922-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-922-10)
1000 TABLET, FILM COATED in 1 BOTTLE (65862-922-99)