| NDC Code | 61919-556-30 |
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| Package Description | 30 TABLET in 1 BOTTLE (61919-556-30) |
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| Product NDC | 61919-556 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pentazocine Hydrochloride And Naloxone Hydrochloride |
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| Non-Proprietary Name | Pentazocine Hydrochloride And Naloxone Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20140101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075735 |
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| Manufacturer | DIRECT RX |
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| Substance Name | PENTAZOCINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
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| Strength | 50; .5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Competitive Opioid Antagonists [MoA],Partial Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
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| DEA Schedule | CIV |
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