NDC 63304-758 – Morphine sulfate
Morphine Sulfate 60 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC63304-758
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 60 mg/1
Uses, dosage, side effects and warnings for Morphine Sulfate →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 63304-758-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-01) | May 11, 2012 |
| 63304-758-03 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-03) | May 11, 2012 |
| 63304-758-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-05) | May 11, 2012 |
| 63304-758-50 | 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-50) | May 11, 2012 |
Recalls mentioning this NDC
- D-0249-2025 Mar 12, 2025 · Class II
Failed Dissolution Specifications
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