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Pentazocine HCl and Acetaminophen
Pentazocine HCl and Acetaminophen - 0591-0396-01 - (Pentazocine HCl and Acetaminophen)
Drug Information of Pentazocine HCl and Acetaminophen
| Product NDC: | 0591-0396 |
| Proprietary Name: | Pentazocine HCl and Acetaminophen |
| Non Proprietary Name: | Pentazocine HCl and Acetaminophen |
| Active Ingredient(s): | 650; 25 mg/1; mg/1 & nbsp; Pentazocine HCl and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pentazocine HCl and Acetaminophen
| Product NDC: | 0591-0396 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074699 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000324 |
Package Information of Pentazocine HCl and Acetaminophen
| Package NDC: | 0591-0396-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0591-0396-01) |
NDC Information of Pentazocine HCl and Acetaminophen
| NDC Code | 0591-0396-01 |
| Proprietary Name | Pentazocine HCl and Acetaminophen |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0591-0396-01) |
| Product NDC | 0591-0396 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pentazocine HCl and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20000324 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE |
| Strength Number | 650; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Competitive Opioid Antagonists [MoA],Partial Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA] |
