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PANADOL
PANADOL - 0135-0150-02 - (acetaminophen and diphenhydramine HCl)
Drug Information of PANADOL
| Product NDC: | 0135-0150 |
| Proprietary Name: | PANADOL |
| Non Proprietary Name: | acetaminophen and diphenhydramine HCl |
| Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; acetaminophen and diphenhydramine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PANADOL
| Product NDC: | 0135-0150 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110323 |
Package Information of PANADOL
| Package NDC: | 0135-0150-02 |
| Package Description: | 50 TABLET, FILM COATED in 1 BOTTLE (0135-0150-02) |
NDC Information of PANADOL
| NDC Code | 0135-0150-02 |
| Proprietary Name | PANADOL |
| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE (0135-0150-02) |
| Product NDC | 0135-0150 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen and diphenhydramine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110323 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
