Good Sense All Day Pain Relief is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Naproxen Sodium.
| Product ID | 63629-1793_5585711c-4a25-4b91-ab53-3fd2ff096054 |
| NDC | 63629-1793 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Good Sense All Day Pain Relief |
| Generic Name | Naproxen Sodium |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1997-01-14 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA079096 |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | NAPROXEN SODIUM |
| Active Ingredient Strength | 220 mg/1 |
| Pharm Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 1997-01-14 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA079096 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-14 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | ANDA |
| Application Number | ANDA079096 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-14 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | ANDA |
| Application Number | ANDA079096 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-14 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | ANDA |
| Application Number | ANDA079096 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-01-14 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | ANDA |
| Application Number | ANDA079096 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-10-09 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | ANDA |
| Application Number | ANDA079096 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-10-09 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | ANDA |
| Application Number | ANDA079096 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-14 |
| Inactivation Date | 2019-11-27 |
| Ingredient | Strength |
|---|---|
| NAPROXEN SODIUM | 220 mg/1 |
| SPL SET ID: | 17f48eda-e036-0673-800f-ca4ef0150059 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 33261-079 | good sense all day pain relief | good sense all day pain relief |
| 50436-6606 | good sense all day pain relief | good sense all day pain relief |
| 63187-104 | good sense all day pain relief | good sense all day pain relief |
| 63629-1793 | Good Sense All Day Pain Relief | Good Sense All Day Pain Relief |
| 66336-002 | good sense all day pain relief | good sense all day pain relief |
| 0280-6000 | Aleve | NAPROXEN SODIUM |
| 0280-6010 | Aleve | NAPROXEN SODIUM |
| 0280-6020 | Aleve | NAPROXEN SODIUM |
| 0280-0041 | Aleve Headache Pain | Naproxen Sodium |
| 0113-7033 | basic care naproxen sodium | Naproxen Sodium |
| 0113-7368 | Basic Care Naproxen Sodium | Naproxen Sodium |
| 0113-7901 | basic care naproxen sodium | Naproxen Sodium |
| 0113-0901 | Good Sense Naproxen Sodium | Naproxen Sodium |
| 0113-1412 | good sense naproxen sodium | naproxen sodium |
| 0113-1773 | good sense naproxen sodium | Naproxen Sodium |
| 0113-4368 | Good Sense Naproxen Sodium | Naproxen Sodium |
| 0280-0270 | Menstridol | NAPROXEN SODIUM |
| 0143-9908 | NAPROXEN | naproxen sodium |
| 0143-9916 | NAPROXEN | naproxen sodium |