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PENTAZOCINE HCL AND NALOXONE HCL
PENTAZOCINE HCL AND NALOXONE HCL - 16590-556-30 - (PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE)
Drug Information of PENTAZOCINE HCL AND NALOXONE HCL
| Product NDC: | 16590-556 |
| Proprietary Name: | PENTAZOCINE HCL AND NALOXONE HCL |
| Non Proprietary Name: | PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE |
| Active Ingredient(s): | .5; 50 mg/1; mg/1 & nbsp; PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PENTAZOCINE HCL AND NALOXONE HCL
| Product NDC: | 16590-556 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074736 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970121 |
Package Information of PENTAZOCINE HCL AND NALOXONE HCL
| Package NDC: | 16590-556-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (16590-556-30) |
NDC Information of PENTAZOCINE HCL AND NALOXONE HCL
| NDC Code | 16590-556-30 |
| Proprietary Name | PENTAZOCINE HCL AND NALOXONE HCL |
| Package Description | 30 TABLET in 1 BOTTLE (16590-556-30) |
| Product NDC | 16590-556 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19970121 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE |
| Strength Number | .5; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Competitive Opioid Antagonists [MoA],Partial Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
