Home NDC 46672-166-50 NDC 46672-166-50 - hydrocodone bitartrate and acetaminophen 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 46672-166
Requested NDC 46672-166-50
Package NDCs from labels 46672-166-10, 46672-166-50
Manufacturer Mikart, LLC
Effective date 2020-12-31
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 HYDROCODONE BITARTRATE ACTIVE INGREDIENT NO70W886KK HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 HYDROCODONE ACTIVE MOIETY 6YKS4Y3WQ7 HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 CROSPOVIDONE INACTIVE INGREDIENT 68401960MK HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 POVIDONES INACTIVE INGREDIENT FZ989GH94E HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [MIKART, INC.] 4
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 67 of 183 · 3,644 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.