| NDC Code | 68084-159-01 |
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| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-159-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-159-11) |
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| Product NDC | 68084-159 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Morphine Sulfate |
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| Proprietary Name Suffix | Extended Release |
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| Non-Proprietary Name | Morphine Sulfate |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20130621 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074862 |
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| Manufacturer | American Health Packaging |
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| Substance Name | MORPHINE SULFATE |
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| Strength | 60 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
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| DEA Schedule | CII |
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