Humana Pharmacy All Day Pain Relief is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Humana Pharmacy, Inc.. The primary component is Naproxen Sodium.
Product ID | 70925-368_e37760dd-14d8-452e-9774-d98d5bc00866 |
NDC | 70925-368 |
Product Type | Human Otc Drug |
Proprietary Name | Humana Pharmacy All Day Pain Relief |
Generic Name | Naproxen Sodium |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2016-12-21 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA074661 |
Labeler Name | Humana Pharmacy, Inc. |
Substance Name | NAPROXEN SODIUM |
Active Ingredient Strength | 220 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2016-12-21 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA074661 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-12-21 |
Ingredient | Strength |
---|---|
NAPROXEN SODIUM | 220 mg/1 |
SPL SET ID: | 5e5049d3-1788-47a1-b419-95d429759f2a |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
70925-368 | Humana Pharmacy All Day Pain Relief | Humana Pharmacy 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 |