Hydromorphone Hydrochloride 71335-0723
Product NDC
71335-0723- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- May 17, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA205814
Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydromorphone Hydrochloride | 4 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(10)
90 TABLET in 1 BOTTLE (71335-0723-0)
30 TABLET in 1 BOTTLE (71335-0723-1)
180 TABLET in 1 BOTTLE (71335-0723-2)
120 TABLET in 1 BOTTLE (71335-0723-3)
20 TABLET in 1 BOTTLE (71335-0723-4)
25 TABLET in 1 BOTTLE (71335-0723-5)
100 TABLET in 1 BOTTLE (71335-0723-6)
60 TABLET in 1 BOTTLE (71335-0723-7)
56 TABLET in 1 BOTTLE (71335-0723-8)
140 TABLET in 1 BOTTLE (71335-0723-9)