| NDC Code | 63304-506-01 |
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| Package Description | 100 TABLET in 1 BOTTLE (63304-506-01) |
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| Product NDC | 63304-506 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pentazocine And Naloxone |
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| Non-Proprietary Name | Pentazocine And Naloxone |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20180731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075523 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | NALOXONE HYDROCHLORIDE; PENTAZOCINE |
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| Strength | .5; 50 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Competitive Opioid Antagonists [MoA], Opioid Antagonist [EPC], Opioid Antagonists [MoA], Partial Opioid Agonist/Antagonist [EPC], Partial Opioid Agonists [MoA] |
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| DEA Schedule | CIV |
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