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acetaminophen and codeine phosphate
acetaminophen and codeine phosphate - 0603-1020-58 - (acetaminophen and codeine phosphate)
Drug Information of acetaminophen and codeine phosphate
| Product NDC: | 0603-1020 |
| 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: | 0603-1020 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089450 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950711 |
Package Information of acetaminophen and codeine phosphate
| Package NDC: | 0603-1020-58 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0603-1020-58) |
NDC Information of acetaminophen and codeine phosphate
| NDC Code | 0603-1020-58 |
| Proprietary Name | acetaminophen and codeine phosphate |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (0603-1020-58) |
| Product NDC | 0603-1020 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acetaminophen and codeine phosphate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19950711 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
| Strength Number | 120; 12 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
