Phenobarbital 51672-5334
Product NDC
51672-5334- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- August 1, 2024
- Listing Expires
- December 31, 2027
Active Ingredients
| Ingredient | Strength |
|---|---|
| Phenobarbital | 100 mg/1 |
Packaging Options(2)
100 TABLET in 1 BOTTLE, PLASTIC (51672-5334-1)
1000 TABLET in 1 BOTTLE, PLASTIC (51672-5334-3)