NDC 79903-098

All Day Back and Muscle Pain Relief

Naproxen Sodium

All Day Back and Muscle Pain Relief is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Walmart Inc.. The primary component is Naproxen Sodium.

Product ID79903-098_017a5bec-48ea-46fc-8af6-779a93a57074
NDC79903-098
Product TypeHuman Otc Drug
Proprietary NameAll Day Back and Muscle Pain Relief
Generic NameNaproxen Sodium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2022-01-17
Marketing CategoryANDA /
Application NumberANDA204872
Labeler NameWALMART INC.
Substance NameNAPROXEN SODIUM
Active Ingredient Strength220 mg/1
Pharm ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 79903-098-06

1 BOTTLE, PLASTIC in 1 CARTON (79903-098-06) > 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing Start Date2022-01-17
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "All Day Back and Muscle Pain Relief" or generic name "Naproxen Sodium"

NDCBrand NameGeneric Name
0280-6000AleveNAPROXEN SODIUM
0280-6010AleveNAPROXEN SODIUM
0280-6020AleveNAPROXEN SODIUM
0280-0041Aleve Headache PainNaproxen Sodium
0113-7033basic care naproxen sodiumNaproxen Sodium
0113-7368Basic Care Naproxen SodiumNaproxen Sodium
0113-7901basic care naproxen sodiumNaproxen Sodium
0113-0901Good Sense Naproxen SodiumNaproxen Sodium
0113-1412good sense naproxen sodiumnaproxen sodium
0113-1773good sense naproxen sodiumNaproxen Sodium
0113-4368Good Sense Naproxen SodiumNaproxen Sodium
0280-0270MenstridolNAPROXEN SODIUM
0143-9908NAPROXENnaproxen sodium
0143-9916NAPROXENnaproxen sodium

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