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Lorcet
Lorcet - 55289-407-20 - (Hydrocodone bitartrate and Acetaminophen)
Drug Information of Lorcet
| Product NDC: | 55289-407 |
| Proprietary Name: | Lorcet |
| Non Proprietary Name: | Hydrocodone bitartrate and Acetaminophen |
| Active Ingredient(s): | 650; 10 mg/1; mg/1 & nbsp; Hydrocodone bitartrate and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lorcet
| Product NDC: | 55289-407 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA081223 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19920529 |
Package Information of Lorcet
| Package NDC: | 55289-407-20 |
| Package Description: | 20 TABLET in 1 BOTTLE, PLASTIC (55289-407-20) |
NDC Information of Lorcet
| NDC Code | 55289-407-20 |
| Proprietary Name | Lorcet |
| Package Description | 20 TABLET in 1 BOTTLE, PLASTIC (55289-407-20) |
| Product NDC | 55289-407 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone bitartrate and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19920529 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 650; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
