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LORTAB
LORTAB - 54868-2908-0 - (Hydrocodone Bitartrate and Acetaminophen)
Drug Information of LORTAB
| Product NDC: | 54868-2908 |
| Proprietary Name: | LORTAB |
| Non Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Active Ingredient(s): | 500; 7.5 mg/15mL; mg/15mL & nbsp; Hydrocodone Bitartrate and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LORTAB
| Product NDC: | 54868-2908 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040520 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19940816 |
Package Information of LORTAB
| Package NDC: | 54868-2908-0 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (54868-2908-0) |
NDC Information of LORTAB
| NDC Code | 54868-2908-0 |
| Proprietary Name | LORTAB |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (54868-2908-0) |
| Product NDC | 54868-2908 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19940816 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 500; 7.5 |
| Strength Unit | mg/15mL; mg/15mL |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
