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arthritis pain relief
arthritis pain relief - 41268-544-71 - (Acetaminophen)
Drug Information of arthritis pain relief
| Product NDC: | 41268-544 |
| Proprietary Name: | arthritis pain relief |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 650 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of arthritis pain relief
| Product NDC: | 41268-544 |
| Labeler Name: | Hannaford Brothers Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075077 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000623 |
Package Information of arthritis pain relief
| Package NDC: | 41268-544-71 |
| Package Description: | 1 BOTTLE in 1 CARTON (41268-544-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
NDC Information of arthritis pain relief
| NDC Code | 41268-544-71 |
| Proprietary Name | arthritis pain relief |
| Package Description | 1 BOTTLE in 1 CARTON (41268-544-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
| Product NDC | 41268-544 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20000623 |
| Marketing Category Name | ANDA |
| Labeler Name | Hannaford Brothers Company |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
