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Acetaminophen and Codeine Phosphate
Acetaminophen and Codeine Phosphate - 0121-0504-05 - (ACETAMINOPHEN and CODEINE PHOSPHATE)
Drug Information of Acetaminophen and Codeine Phosphate
| Product NDC: | 0121-0504 |
| Proprietary Name: | Acetaminophen and Codeine Phosphate |
| Non Proprietary Name: | ACETAMINOPHEN and CODEINE PHOSPHATE |
| Active Ingredient(s): | 120; 12 mg/5mL; mg/5mL & nbsp; ACETAMINOPHEN and CODEINE PHOSPHATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acetaminophen and Codeine Phosphate
| Product NDC: | 0121-0504 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087508 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19810821 |
Package Information of Acetaminophen and Codeine Phosphate
| Package NDC: | 0121-0504-05 |
| Package Description: | 10 TRAY in 1 CASE (0121-0504-05) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
NDC Information of Acetaminophen and Codeine Phosphate
| NDC Code | 0121-0504-05 |
| Proprietary Name | Acetaminophen and Codeine Phosphate |
| Package Description | 10 TRAY in 1 CASE (0121-0504-05) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 0121-0504 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ACETAMINOPHEN and CODEINE PHOSPHATE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19810821 |
| Marketing Category Name | ANDA |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
| Strength Number | 120; 12 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
