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PANADOL
PANADOL - 0135-0135-03 - (acetaminophen)
Drug Information of PANADOL
| Product NDC: | 0135-0135 |
| Proprietary Name: | PANADOL |
| Non Proprietary Name: | acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PANADOL
| Product NDC: | 0135-0135 |
| Labeler Name: | GlaxoSmithKline Consumer Healtcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110318 |
Package Information of PANADOL
| Package NDC: | 0135-0135-03 |
| Package Description: | 60 TABLET in 1 BOTTLE (0135-0135-03) |
NDC Information of PANADOL
| NDC Code | 0135-0135-03 |
| Proprietary Name | PANADOL |
| Package Description | 60 TABLET in 1 BOTTLE (0135-0135-03) |
| Product NDC | 0135-0135 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110318 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healtcare LP |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
