Home NDC 50474-925-01 NDC 50474-925-01 - Lortab 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 50474-925
Requested NDC 50474-925-01
Package NDCs from labels 50474-925-01, 50474-925-50
Manufacturer UCB PHARMA, INC.
Effective date 2006-10-20
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Lortab - UCB PHARMA, INC. UCB PHARMA, INC. 2006-10-20 Human prescription drug label
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50474-925-01 Lortab 100 in 1 BOTTLE, PLASTIC TABLET 100 1 50474-925-50 Lortab 500 in 1 BOTTLE, PLASTIC TABLET 500 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50474-925 LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 2 package rows 20061201_1FB18A80-8EF0-4BCE-BB0D-9A86851C5206.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 Hydrocodone bitartrate ACTIVE INGREDIENT NO70W886KK LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 Hydrocodone ACTIVE MOIETY 6YKS4Y3WQ7 LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 COLLOIDAL SILICON DIOXIDE INACTIVE INGREDIENT LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 CROSPOVIDONE INACTIVE INGREDIENT LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 FD & C RED #3 INACTIVE INGREDIENT LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 MICROCRYSTALLINE CELLULOSE INACTIVE INGREDIENT LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 POVIDONE INACTIVE INGREDIENT LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 PREGELATINIZED STARCH INACTIVE INGREDIENT LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 SUCROSE INACTIVE INGREDIENT C151H8M554 LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1 SUGAR SPHERES INACTIVE INGREDIENT LORTAB (HYDROCODONE BITARTRATE AND ACETAMINOPHEN) TABLET [UCB PHARMA, INC.] 1
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.