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ACETAMINOPHEN AND CODEINE PHOSPHATE
ACETAMINOPHEN AND CODEINE PHOSPHATE - 60432-245-16 - (Acetaminophen and Codeine Phosphate)
Drug Information of ACETAMINOPHEN AND CODEINE PHOSPHATE
| Product NDC: | 60432-245 |
| 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: | 60432-245 |
| Labeler Name: | Morton Grove Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087006 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19810722 |
Package Information of ACETAMINOPHEN AND CODEINE PHOSPHATE
| Package NDC: | 60432-245-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (60432-245-16) |
NDC Information of ACETAMINOPHEN AND CODEINE PHOSPHATE
| NDC Code | 60432-245-16 |
| Proprietary Name | ACETAMINOPHEN AND CODEINE PHOSPHATE |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (60432-245-16) |
| Product NDC | 60432-245 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acetaminophen and Codeine Phosphate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19810722 |
| Marketing Category Name | ANDA |
| Labeler Name | Morton Grove Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
| Strength Number | 120; 12 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
