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Lorcet Plus
Lorcet Plus - 0785-1122-50 - (hydrocodone bitartrate and acetaminophen)
Drug Information of Lorcet Plus
| Product NDC: | 0785-1122 |
| Proprietary Name: | Lorcet Plus |
| Non Proprietary Name: | hydrocodone bitartrate and acetaminophen |
| Active Ingredient(s): | 650; 7.5 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 Plus
| Product NDC: | 0785-1122 |
| Labeler Name: | Forest Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089689 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19841231 |
Package Information of Lorcet Plus
| Package NDC: | 0785-1122-50 |
| Package Description: | 500 TABLET in 1 BOTTLE, PLASTIC (0785-1122-50) |
NDC Information of Lorcet Plus
| NDC Code | 0785-1122-50 |
| Proprietary Name | Lorcet Plus |
| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (0785-1122-50) |
| Product NDC | 0785-1122 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocodone bitartrate and acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19841231 |
| Marketing Category Name | ANDA |
| Labeler Name | Forest Laboratories, Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 650; 7.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
