Hydromorphone Hydrochloride 60687-0590
Product NDC
60687-0590- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- May 11, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA076855
Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydromorphone Hydrochloride | 4 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(1)
100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-590-01) / 1 TABLET in 1 BLISTER PACK (60687-590-11)