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Acetaminophen and Codeine
Acetaminophen and Codeine - 50436-3227-2 - (Acetaminophen and Codeine)
Drug Information of Acetaminophen and Codeine
| Product NDC: | 50436-3227 |
| Proprietary Name: | Acetaminophen and Codeine |
| Non Proprietary Name: | Acetaminophen and Codeine |
| Active Ingredient(s): | 300; 30 mg/1; mg/1 & nbsp; Acetaminophen and Codeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acetaminophen and Codeine
| Product NDC: | 50436-3227 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040779 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080529 |
Package Information of Acetaminophen and Codeine
| Package NDC: | 50436-3227-2 |
| Package Description: | 20 TABLET in 1 BOTTLE (50436-3227-2) |
NDC Information of Acetaminophen and Codeine
| NDC Code | 50436-3227-2 |
| Proprietary Name | Acetaminophen and Codeine |
| Package Description | 20 TABLET in 1 BOTTLE (50436-3227-2) |
| Product NDC | 50436-3227 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acetaminophen and Codeine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080529 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | ACETAMINOPHEN; CODEINE |
| Strength Number | 300; 30 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
