| NDC Code | 67046-996-30 |
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| Package Description | 30 TABLET in 1 BLISTER PACK (67046-996-30) |
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| Product NDC | 67046-996 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Buprenorphine Hydrochloride Sublingual |
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| Non-Proprietary Name | Buprenorphine Hydrochloride Sublingual |
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| Dosage Form | TABLET |
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| Usage | SUBLINGUAL |
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| Start Marketing Date | 20150306 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201066 |
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| Manufacturer | Contract Pharmacy Services-PA |
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| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
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| Strength | 2 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC] |
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| DEA Schedule | CIII |
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