NDC 42858-802 – Morphine Sulfate Extended Release
Morphine Sulfate 30 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC42858-802
Product details
- Brand name
- Morphine Sulfate Extended Release
- Generic name
- Morphine Sulfate
- Labeler
- Rhodes Pharmaceuticals LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA074862
- Marketed since
- January 14, 2011
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Morphine Sulfate 30 mg/1
Uses, dosage, side effects and warnings for Morphine Sulfate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 42858-802-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42858-802-01) | Jan 14, 2011 |
Other Morphine Sulfate products
- 0228-3092 Morphine Sulfate 90 mg/1 · Capsule, Extended Release · Actavis Pharma, Inc.
- 0228-3117 Morphine Sulfate 75 mg/1 · Capsule, Extended Release · Actavis Pharma, Inc.
- 0228-3093 Morphine Sulfate 120 mg/1 · Capsule, Extended Release · Actavis Pharma, Inc.
- 0228-3091 Morphine Sulfate 60 mg/1 · Capsule, Extended Release · Actavis Pharma, Inc.
- 0228-3116 Morphine Sulfate 45 mg/1 · Capsule, Extended Release · Actavis Pharma, Inc.
- 0228-3090 Morphine Sulfate 30 mg/1 · Capsule, Extended Release · Actavis Pharma, Inc.
- 68000-111 Morphine Sulfate 20 mg/mL · Solution · American Health Packaging
- 60687-617 Morphine Sulfate 15 mg/1 · Tablet · American Health Packaging
- 60687-760 Morphine Sulfate 10 mg/5mL · Solution · American Health Packaging
- 60687-927 Morphine Sulfate 10 mg/5mL · Solution · American Health Packaging
- 68000-110 Morphine Sulfate 20 mg/mL · Solution · American Health Packaging
- 68000-112 Morphine Sulfate 20 mg/mL · Solution · American Health Packaging