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Goodys
Goodys - 10158-003-08 - (acetaminophen and diphenhydramine citrate)
Drug Information of Goodys
| Product NDC: | 10158-003 |
| Proprietary Name: | Goodys |
| Non Proprietary Name: | acetaminophen and diphenhydramine citrate |
| Active Ingredient(s): | 500; 38 mg/1; mg/1 & nbsp; acetaminophen and diphenhydramine citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Goodys
| Product NDC: | 10158-003 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110919 |
Package Information of Goodys
| Package NDC: | 10158-003-08 |
| Package Description: | 6 POWDER in 1 PACKAGE (10158-003-08) |
NDC Information of Goodys
| NDC Code | 10158-003-08 |
| Proprietary Name | Goodys |
| Package Description | 6 POWDER in 1 PACKAGE (10158-003-08) |
| Product NDC | 10158-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen and diphenhydramine citrate |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20110919 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE CITRATE |
| Strength Number | 500; 38 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
