Hydromorphone Hydrochloride 00406-3249
Product NDC
00406-3249- Manufacturer
- Specgx Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- December 23, 2004
- Listing Expires
- December 31, 2026
- Application
- ANDA076855
Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydromorphone Hydrochloride | 8 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
100 TABLET in 1 BOTTLE (0406-3249-01)