NDC 43386-541 – Morphine Sulfate
Morphine Sulfate 30 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC43386-541
Product details
- Brand name
- Morphine Sulfate
- Generic name
- Morphine Sulfate
- Labeler
- Lupin Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA203602
- Marketed since
- December 16, 2015
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 43386-541-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43386-541-01) | Dec 16, 2015 |
Recalls mentioning this NDC
- D-1246-2019 May 1, 2019 · Class III
Failed Impurities/Degradation Specifications - D-1247-2019 May 1, 2019 · Class III
Failed Impurities/Degradation Specifications - D-1243-2019 May 1, 2019 · Class III
Failed Impurities/Degradation Specifications - D-1245-2019 May 1, 2019 · Class III
Failed Impurities/Degradation Specifications - D-1244-2019 May 1, 2019 · Class III
Failed Impurities/Degradation Specifications - D-1214-2018 Sep 26, 2018 · Class III
Failed Impurities/Degradation Specifications: Morphine Sulfate Extended Release Tablets are being recalled due to out of Specification Result noticed for Morphinone Sulfate impurity during 3 month…
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