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fever reducing
fever reducing - 59779-579-53 - (Acetaminophen)
Drug Information of fever reducing
| Product NDC: | 59779-579 |
| Proprietary Name: | fever reducing |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 120 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of fever reducing
| Product NDC: | 59779-579 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA070607 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100121 |
Package Information of fever reducing
| Package NDC: | 59779-579-53 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (59779-579-53) > 6 SUPPOSITORY in 1 BLISTER PACK |
NDC Information of fever reducing
| NDC Code | 59779-579-53 |
| Proprietary Name | fever reducing |
| Package Description | 2 BLISTER PACK in 1 CARTON (59779-579-53) > 6 SUPPOSITORY in 1 BLISTER PACK |
| Product NDC | 59779-579 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 20100121 |
| Marketing Category Name | ANDA |
| Labeler Name | CVS Pharmacy |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
