Pain Relief All Day is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Naproxen Sodium.
Product ID | 0363-0490_30ff32dc-9da2-429d-963b-fea6dd02d5ae |
NDC | 0363-0490 |
Product Type | Human Otc Drug |
Proprietary Name | Pain Relief All Day |
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 | ANDA074661 |
Labeler Name | Walgreen Company |
Substance Name | NAPROXEN SODIUM |
Active Ingredient Strength | 220 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 1997-01-14 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA074661 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-10-06 |
Marketing Category | ANDA |
Application Number | ANDA074661 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-01-14 |
Marketing Category | ANDA |
Application Number | ANDA074661 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-01-14 |
Marketing Category | ANDA |
Application Number | ANDA074661 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-01-14 |
Marketing Category | ANDA |
Application Number | ANDA074661 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2002-06-20 |
Ingredient | Strength |
---|---|
NAPROXEN SODIUM | 220 mg/1 |
SPL SET ID: | d2858775-de6a-4e14-b100-294ec9b074d4 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |