Baclofen 71335-0949
Product NDC
71335-0949- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 1, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA209102
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Baclofen | 20 mg/1 |
Drug Class
gamma-Aminobutyric Acid-ergic Agonist [EPC]GABA A Agonists [MoA]GABA B Agonists [MoA]
Packaging Options(10)
120 TABLET in 1 BOTTLE (71335-0949-0)
90 TABLET in 1 BOTTLE (71335-0949-1)
20 TABLET in 1 BOTTLE (71335-0949-2)
60 TABLET in 1 BOTTLE (71335-0949-3)
45 TABLET in 1 BOTTLE (71335-0949-4)
112 TABLET in 1 BOTTLE (71335-0949-5)
30 TABLET in 1 BOTTLE (71335-0949-6)
56 TABLET in 1 BOTTLE (71335-0949-7)
15 TABLET in 1 BOTTLE (71335-0949-8)
84 TABLET in 1 BOTTLE (71335-0949-9)