Home
>
National Drug Code (NDC)
>
Sunmark Arthritis Pain Reliever
Sunmark Arthritis Pain Reliever - 49348-921-10 - (Acetaminophen)
Drug Information of Sunmark Arthritis Pain Reliever
| Product NDC: | 49348-921 |
| Proprietary Name: | Sunmark Arthritis Pain Reliever |
| 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 Sunmark Arthritis Pain Reliever
| Product NDC: | 49348-921 |
| Labeler Name: | Sunmark |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076200 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020430 |
Package Information of Sunmark Arthritis Pain Reliever
| Package NDC: | 49348-921-10 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-10) |
NDC Information of Sunmark Arthritis Pain Reliever
| NDC Code | 49348-921-10 |
| Proprietary Name | Sunmark Arthritis Pain Reliever |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-10) |
| Product NDC | 49348-921 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20020430 |
| Marketing Category Name | ANDA |
| Labeler Name | Sunmark |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
