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Arthriten
Arthriten - 52389-237-28 - (acetaminophen, aspirin, caffeine)
Drug Information of Arthriten
| Product NDC: | 52389-237 |
| Proprietary Name: | Arthriten |
| Non Proprietary Name: | acetaminophen, aspirin, caffeine |
| Active Ingredient(s): | 250; 250; 65 mg/1; mg/1; mg/1 & nbsp; acetaminophen, aspirin, caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arthriten
| Product NDC: | 52389-237 |
| Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120723 |
Package Information of Arthriten
| Package NDC: | 52389-237-28 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (52389-237-28) > 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52389-237-01) |
NDC Information of Arthriten
| NDC Code | 52389-237-28 |
| Proprietary Name | Arthriten |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (52389-237-28) > 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52389-237-01) |
| Product NDC | 52389-237 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen, aspirin, caffeine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120723 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
| Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
| Strength Number | 250; 250; 65 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
