Home
>
National Drug Code (NDC)
>
pain relief
pain relief - 50804-016-00 - (Acetaminophen)
Drug Information of pain relief
| Product NDC: | 50804-016 |
| Proprietary Name: | pain relief |
| 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 pain relief
| Product NDC: | 50804-016 |
| Labeler Name: | Geiss, Destin & Dunn, Inc (Goodsense) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111115 |
Package Information of pain relief
| Package NDC: | 50804-016-00 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (50804-016-00) > 100 TABLET in 1 BOTTLE, PLASTIC |
NDC Information of pain relief
| NDC Code | 50804-016-00 |
| Proprietary Name | pain relief |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50804-016-00) > 100 TABLET in 1 BOTTLE, PLASTIC |
| Product NDC | 50804-016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111115 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Geiss, Destin & Dunn, Inc (Goodsense) |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
