NDC 68788-7572

Naproxen

Naproxen Sodium

Naproxen is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is Naproxen Sodium.

Product ID68788-7572_20eb9d9f-11df-464f-a1b0-949f8fda4042
NDC68788-7572
Product TypeHuman Otc Drug
Proprietary NameNaproxen
Generic NameNaproxen Sodium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2019-01-01
Marketing CategoryANDA / ANDA
Application NumberANDA204872
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NameNAPROXEN SODIUM
Active Ingredient Strength220 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 68788-7572-2

20 TABLET in 1 BOTTLE (68788-7572-2)
Marketing Start Date2019-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-7572-6 [68788757206]

Naproxen TABLET
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 68788-7572-3 [68788757203]

Naproxen TABLET
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 68788-7572-2 [68788757202]

Naproxen TABLET
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 68788-7572-4 [68788757204]

Naproxen TABLET
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

Drug Details

Active Ingredients

IngredientStrength
NAPROXEN SODIUM220 mg/1

NDC Crossover Matching brand name "Naproxen" or generic name "Naproxen Sodium"

NDCBrand NameGeneric Name
0054-3630NaproxenNaproxen
0093-1005NaproxenNaproxen
0093-1006NaproxenNaproxen
0143-1346NaproxenNaproxen
0143-1347NaproxenNaproxen
0143-1348NaproxenNaproxen
0143-9908NAPROXENnaproxen sodium
0143-9916NAPROXENnaproxen sodium
0179-1978NaproxenNaproxen
68071-3092NaproxenNaproxen
68071-4006NAPROXENNAPROXEN
68071-3029naproxennaproxen
68071-3066naproxennaproxen
68071-3387NaproxenNaproxen
68071-3345NAPROXENNAPROXEN
68071-4510NAPROXENNAPROXEN
68071-4381NAPROXENNAPROXEN
0440-1852NaproxenNaproxen
68134-201NaproxenNaproxen
0440-7852NaproxenNaproxen
68151-2894NaproxenNaproxen
68151-2609NaproxenNaproxen
68151-2895NaproxenNaproxen
68382-012NaproxenNaproxen
68382-013NaproxenNaproxen
68382-014NaproxenNaproxen
68387-800NaproxenNaproxen
68387-801NaproxenNaproxen
68387-802NaproxenNaproxen
68462-190NaproxenNaproxen
68462-189NaproxenNaproxen
68462-188NaproxenNaproxen
68788-6421NaproxenNaproxen
68788-6908NaproxenNaproxen
68788-6998NAPROXENNAPROXEN
68788-7072NaproxenNaproxen
68788-9151NaproxenNaproxen
68788-7090NaproxenNaproxen
68788-6842NaproxenNaproxen
68788-9906NaproxenNaproxen
68788-9878NaproxenNaproxen
68788-9907NaproxenNaproxen
69097-852NaproxenNaproxen
69150-139NAPROXENNAPROXEN
69150-140NAPROXENNAPROXEN
69097-855naproxennaproxen
69097-854naproxennaproxen
69150-138NAPROXENNAPROXEN
69097-851NaproxenNaproxen
69097-853naproxennaproxen

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.