Butalbital And Acetaminophen 68047-0721
Product NDC
68047-0721- Manufacturer
- Larken Laboratories, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- December 4, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA203484
Active Ingredients
| Ingredient | Strength |
|---|---|
| Acetaminophen | 325 mg/1 |
| Butalbital | 50 mg/1 |
Drug Class
Barbiturate [EPC]Barbiturate [EPC]Barbiturates [CS]
Packaging Options(2)
100 TABLET in 1 BOTTLE (68047-721-01)
30 TABLET in 1 BOTTLE (68047-721-30)