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Panadol
Panadol - 0135-0507-04 - (acetaminophen)
Drug Information of Panadol
| Product NDC: | 0135-0507 |
| Proprietary Name: | Panadol |
| Non Proprietary Name: | acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Panadol
| Product NDC: | 0135-0507 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110621 |
Package Information of Panadol
| Package NDC: | 0135-0507-04 |
| Package Description: | 1 BOTTLE in 1 CARTON (0135-0507-04) > 20 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of Panadol
| NDC Code | 0135-0507-04 |
| Proprietary Name | Panadol |
| Package Description | 1 BOTTLE in 1 CARTON (0135-0507-04) > 20 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 0135-0507 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110621 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
