NDC 63304-451 – Morphine sulfate
Morphine Sulfate 30 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC63304-451
Product details
- Brand name
- Morphine sulfate
- Generic name
- morphine sulfate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078761
- Marketed since
- May 11, 2012
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 63304-451-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-451-01) | May 11, 2012 |
| 63304-451-03 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-451-03) | May 11, 2012 |
| 63304-451-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-451-05) | May 11, 2012 |
Recalls mentioning this NDC
- D-0249-2025 Mar 12, 2025 · Class II
Failed Dissolution Specifications
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.
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