Hydromorphone Hydrochloride 42858-0301
Product NDC
42858-0301- Manufacturer
- Rhodes Pharmaceuticals Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- November 23, 2009
- Listing Expires
- December 31, 2027
- Application
- NDA019892
Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydromorphone Hydrochloride | 2 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE, PLASTIC (42858-301-01)
4 BLISTER PACK in 1 CARTON (42858-301-25) / 25 TABLET in 1 BLISTER PACK