Hydromorphone Hydrochloride 71335-9701
Product NDC
71335-9701- Manufacturer
- Bryant Ranch Prepack
- 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 | 4 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(10)
90 TABLET in 1 BOTTLE, PLASTIC (71335-9701-0)
30 TABLET in 1 BOTTLE, PLASTIC (71335-9701-1)
180 TABLET in 1 BOTTLE, PLASTIC (71335-9701-2)
120 TABLET in 1 BOTTLE, PLASTIC (71335-9701-3)
20 TABLET in 1 BOTTLE, PLASTIC (71335-9701-4)
25 TABLET in 1 BOTTLE, PLASTIC (71335-9701-5)
100 TABLET in 1 BOTTLE, PLASTIC (71335-9701-6)
60 TABLET in 1 BOTTLE, PLASTIC (71335-9701-7)
56 TABLET in 1 BOTTLE, PLASTIC (71335-9701-8)
140 TABLET in 1 BOTTLE, PLASTIC (71335-9701-9)