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ACETAMINOPHEN AND CODEINE PHOSPHATE
ACETAMINOPHEN AND CODEINE PHOSPHATE - 24236-009-14 - (acetaminophen and codeine phosphate)
Drug Information of ACETAMINOPHEN AND CODEINE PHOSPHATE
| Product NDC: | 24236-009 |
| Proprietary Name: | ACETAMINOPHEN AND CODEINE PHOSPHATE |
| Non Proprietary Name: | acetaminophen and codeine phosphate |
| Active Ingredient(s): | 300 mg/1 & nbsp; acetaminophen and codeine phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACETAMINOPHEN AND CODEINE PHOSPHATE
| Product NDC: | 24236-009 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040419 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130404 |
Package Information of ACETAMINOPHEN AND CODEINE PHOSPHATE
| Package NDC: | 24236-009-14 |
| Package Description: | 2 TABLET in 1 CARTON (24236-009-14) |
NDC Information of ACETAMINOPHEN AND CODEINE PHOSPHATE
| NDC Code | 24236-009-14 |
| Proprietary Name | ACETAMINOPHEN AND CODEINE PHOSPHATE |
| Package Description | 2 TABLET in 1 CARTON (24236-009-14) |
| Product NDC | 24236-009 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acetaminophen and codeine phosphate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130404 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
