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members mark arthritis pain
members mark arthritis pain - 68196-544-82 - (Acetaminophen)
Drug Information of members mark arthritis pain
| Product NDC: | 68196-544 |
| Proprietary Name: | members mark arthritis pain |
| 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 members mark arthritis pain
| Product NDC: | 68196-544 |
| Labeler Name: | Sam's West Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075077 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050831 |
Package Information of members mark arthritis pain
| Package NDC: | 68196-544-82 |
| Package Description: | 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68196-544-82) |
NDC Information of members mark arthritis pain
| NDC Code | 68196-544-82 |
| Proprietary Name | members mark arthritis pain |
| Package Description | 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68196-544-82) |
| Product NDC | 68196-544 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20050831 |
| Marketing Category Name | ANDA |
| Labeler Name | Sam's West Inc |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
