Morphine Sulfate 63304-0450
Product NDC
63304-0450- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- May 11, 2012
- Listing Expires
- December 31, 2027
- Application
- ANDA078761
Active Ingredients
| Ingredient | Strength |
|---|---|
| Morphine Sulfate | 15 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(3)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-450-01)
10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-450-03)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-450-05)