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ACETAMINOPHEN
ACETAMINOPHEN - 54868-4991-0 - (acetaminophen)
Drug Information of ACETAMINOPHEN
| Product NDC: | 54868-4991 |
| Proprietary Name: | ACETAMINOPHEN |
| Non Proprietary Name: | acetaminophen |
| Active Ingredient(s): | 650 mg/1 & nbsp; acetaminophen |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACETAMINOPHEN
| Product NDC: | 54868-4991 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA070608 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040203 |
Package Information of ACETAMINOPHEN
| Package NDC: | 54868-4991-0 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (54868-4991-0) > 6 SUPPOSITORY in 1 BLISTER PACK |
NDC Information of ACETAMINOPHEN
| NDC Code | 54868-4991-0 |
| Proprietary Name | ACETAMINOPHEN |
| Package Description | 2 BLISTER PACK in 1 CARTON (54868-4991-0) > 6 SUPPOSITORY in 1 BLISTER PACK |
| Product NDC | 54868-4991 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 20040203 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
