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acetaminophen
acetaminophen - 45802-730-32 - (Acetaminophen)
Drug Information of acetaminophen
| Product NDC: | 45802-730 |
| 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: | 45802-730 |
| Labeler Name: | Perrigo New York Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA070608 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101028 |
Package Information of acetaminophen
| Package NDC: | 45802-730-32 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (45802-730-32) > 5 SUPPOSITORY in 1 BLISTER PACK |
NDC Information of acetaminophen
| NDC Code | 45802-730-32 |
| Proprietary Name | acetaminophen |
| Package Description | 10 BLISTER PACK in 1 CARTON (45802-730-32) > 5 SUPPOSITORY in 1 BLISTER PACK |
| Product NDC | 45802-730 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 20101028 |
| Marketing Category Name | ANDA |
| Labeler Name | Perrigo New York Inc |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
