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LORTAB
LORTAB - 16590-636-62 - (HYDROCODONE BITARTRATE AND ACETAMINOPHEN)
Drug Information of LORTAB
| Product NDC: | 16590-636 |
| Proprietary Name: | LORTAB |
| Non Proprietary Name: | HYDROCODONE BITARTRATE AND ACETAMINOPHEN |
| Active Ingredient(s): | 500; 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 LORTAB
| Product NDC: | 16590-636 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089699 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19890825 |
Package Information of LORTAB
| Package NDC: | 16590-636-62 |
| Package Description: | 84 TABLET in 1 BOTTLE (16590-636-62) |
NDC Information of LORTAB
| NDC Code | 16590-636-62 |
| Proprietary Name | LORTAB |
| Package Description | 84 TABLET in 1 BOTTLE (16590-636-62) |
| Product NDC | 16590-636 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCODONE BITARTRATE AND ACETAMINOPHEN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19890825 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 500; 7.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
