Meperidine Hydrochloride 64950-0214
Product NDC
64950-0214- Manufacturer
- Genus Lifesciences Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- February 14, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA040893
Active Ingredients
| Ingredient | Strength |
|---|---|
| Meperidine Hydrochloride | 50 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE, PLASTIC (64950-214-01)
30 TABLET in 1 BOTTLE, PLASTIC (64950-214-03)