Tramadol Hydrochloride 47335-0861
Product NDC
47335-0861- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- December 12, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA201384
Active Ingredients
| Ingredient | Strength |
|---|---|
| Tramadol Hydrochloride | 300 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(4)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-08)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-18)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-83)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-88)