arthritis pain reliever is a Oral Tablet, Film Coated, Extended Release in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Acetaminophen.
| Product ID | 0363-0544_83543ced-27a8-442e-a883-4e7d18405179 |
| NDC | 0363-0544 |
| Product Type | Human Otc Drug |
| Proprietary Name | arthritis pain reliever |
| Generic Name | Acetaminophen |
| Dosage Form | Tablet, Film Coated, Extended Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2000-05-26 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA075077 |
| Labeler Name | Walgreen Company |
| Substance Name | ACETAMINOPHEN |
| Active Ingredient Strength | 650 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 2014-08-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA075077 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-02-11 |
| Marketing End Date | 2013-04-23 |
| Marketing Category | ANDA |
| Application Number | ANDA075077 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-08-15 |
| Marketing Category | ANDA |
| Application Number | ANDA075077 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-02-11 |
| Marketing Category | ANDA |
| Application Number | ANDA075077 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075077 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-02-04 |
| Marketing End Date | 2017-03-23 |
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 650 mg/1 |
| SPL SET ID: | 5028c116-d0e3-4e30-8fa8-caaf08d99ec7 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |