Home NDC 51688-9671 NDC 51688-9671 - 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD 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 51688-9671
Package NDCs from labels 51688-9671-2
Manufacturer Smiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd. | Aplicare, Inc.
Effective date 2016-10-21
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 BUPIVACAINE HYDROCHLORIDE ACTIVE INGREDIENT 7TQO7W3VT8 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 EPINEPHRINE ACTIVE INGREDIENT YKH834O4BH 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 LIDOCAINE HYDROCHLORIDE ANHYDROUS ACTIVE INGREDIENT EC2CNF7XFP 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 POVIDONE-IODINE ACTIVE INGREDIENT 85H0HZU99M 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 BUPIVACAINE ACTIVE MOIETY Y8335394RO 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 EPINEPHRINE ACTIVE MOIETY YKH834O4BH 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 IODINE ACTIVE MOIETY 9679TC07X4 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 Lidocaine ACTIVE MOIETY 98PI200987 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 SODIUM CATION ACTIVE MOIETY LYR4M0NH37 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 ANHYDROUS CITRIC ACID INACTIVE INGREDIENT XF417D3PSL 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 Hydrochloric Acid INACTIVE INGREDIENT QTT17582CB 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 NONOXYNOL-9 INACTIVE INGREDIENT 48Q180SH9T 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 Sodium Chloride INACTIVE INGREDIENT 451W47IQ8X 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 Sodium Hydroxide INACTIVE INGREDIENT 55X04QC32I 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 SODIUM METABISULFITE INACTIVE INGREDIENT 4VON5FNS3C 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 SODIUM PHOSPHATE, DIBASIC INACTIVE INGREDIENT GR686LBA74 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1 Water INACTIVE INGREDIENT 059QF0KO0R 15957-20 CONTINUOUS EPIDURAL 18G CRAWFORD/18G HUSTEAD () KIT [SMITHS MEDICAL ASD, INC.] 1
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 108 of 108 · 2,143 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join TIS-U-SOL SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE Baxter Healthcare Corporation 9da4121f-d62d-4da4-8dfb-0494da16015f 2014-02-21 Exact identifier unii: 451W47IQ8X Ringers SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, Baxter Healthcare Corporation e1953d54-818d-46a6-8532-518ebae6d84e 2012-06-13 Exact identifier unii: 451W47IQ8X Lactated Ringers SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE Baxter Healthcare Corporation f09f80bf-2f8b-4420-865d-aec2d5e5cd4d 2012-06-12 Exact identifier unii: 451W47IQ8X
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.