Home NDC 62037-930-05 NDC 62037-930-05 - PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 62037-930
Requested NDC 62037-930-05
Package NDCs from labels 62037-930-01, 62037-930-05
Manufacturer Andrx Pharmaceuticals, Inc.
Effective date 2008-11-18
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62037-930-01 PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN 100 in 1 BOTTLE TABLET, FILM COATED 100 1 62037-930-05 PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN 500 in 1 BOTTLE TABLET, FILM COATED 500 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62037-930 PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 2 package rows 20081211_7b3e3fee-b02a-4898-a45e-e4abc1e8d9f4.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Acetaminophen ACTIVE INGREDIENT 362O9ITL9D PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 Propoxyphene Napsylate ACTIVE INGREDIENT 38M219L1OJ PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 acetaminophen ACTIVE MOIETY 362O9ITL9D PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 propoxyphene ACTIVE MOIETY S2F83W92TK PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 colloidal silicon dioxide INACTIVE INGREDIENT ETJ7Z6XBU4 PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 croscarmellose sodium INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 crospovidone INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 FD&C Red #40 Aluminum Lake INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 FD&C Yellow #6 Aluminum Lake INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 hypromellose 2910 3cP INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 hypromellose 2910 50cP INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 hypromellose 2910 6cP INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 magnesium stearate INACTIVE INGREDIENT 70097M6I30 PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 microcrystalline cellulose INACTIVE INGREDIENT OP1R32D61U PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 polydextrose INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 polyethylene glycol 400 INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 polyethylene glycol 8000 INACTIVE INGREDIENT PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 stearic acid INACTIVE INGREDIENT 4ELV7Z65AP PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 titanium dioxide INACTIVE INGREDIENT 15FIX9V2JP PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1 triacetin INACTIVE INGREDIENT XHX3C3X673 PROPOXYPHENE NAPSYLATE AND ACETOMINOPHEN TABLET, FILM COATED [ANDRX PHARMACEUTICALS, INC.] 1
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