NDC 51688-9656-2 - 15922-20 CONTINUOUS EPIDURAL 18G TUOHY

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: 51688-9656
Requested NDC: 51688-9656-2
Package NDCs from labels: 51688-9656-2
Manufacturer: Smiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd. | Aplicare, Inc.
Effective date: 2014-09-24
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
15922-20 CONTINUOUS EPIDURAL 18G TUOHY	Smiths Medical ASD, Inc. \| Hospira, Inc. \| Kwang Myung Pharm. Co., Ltd. \| Aplicare, Inc.	2014-09-24	MEDICAL DEVICE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BUPIVACAINE HYDROCHLORIDE	ACTIVE INGREDIENT	7TQO7W3VT8	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
EPINEPHRINE	ACTIVE INGREDIENT	YKH834O4BH	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
LIDOCAINE HYDROCHLORIDE	ACTIVE INGREDIENT	V13007Z41A	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
POVIDONE-IODINE	ACTIVE INGREDIENT	85H0HZU99M	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
SODIUM CHLORIDE	ACTIVE INGREDIENT	451W47IQ8X	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
BUPIVACAINE	ACTIVE MOIETY	Y8335394RO	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
CHLORIDE ION	ACTIVE MOIETY	Q32ZN48698	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
EPINEPHRINE	ACTIVE MOIETY	YKH834O4BH	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
IODINE	ACTIVE MOIETY	9679TC07X4	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
LIDOCAINE	ACTIVE MOIETY	98PI200987	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
Hydrochloric Acid	INACTIVE INGREDIENT	QTT17582CB	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
NONOXYNOL-9	INACTIVE INGREDIENT	48Q180SH9T	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
Sodium Chloride	INACTIVE INGREDIENT	451W47IQ8X	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
Sodium Hydroxide	INACTIVE INGREDIENT	55X04QC32I	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
SODIUM METABISULFITE	INACTIVE INGREDIENT	4VON5FNS3C	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
SODIUM PHOSPHATE, DIBASIC	INACTIVE INGREDIENT	GR686LBA74	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2
Water	INACTIVE INGREDIENT	059QF0KO0R	15922-20 CONTINUOUS EPIDURAL 18G TUOHY () C47916 [SMITHS MEDICAL ASD, INC.]	2

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 111 of 113 · 2,260 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lidocaine Hydrochloride	LIDOCAINE HYDROCHLORIDE	Asclemed USA, Inc.	b8803e38-fe30-48ec-9399-013f2880e0eb	2020-04-09	Warnings, Adverse reactions	Exact identifier unii: V13007Z41A
Bupivacaine Hydrochloride	BUPIVACAINE HYDROCHLORIDE	Asclemed USA, Inc.	3eefbefe-78ae-4f2d-9be6-3f79eadcff86	2020-04-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 7TQO7W3VT8
0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE	HF Acquisition Co LLC, DBA HealthFirst	a2b8220f-e33a-51c3-e053-2995a90a0734	2020-04-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE	HF Acquisition Co LLC, DBA HealthFirst	a2bba76a-08ce-6902-e053-2995a90ab9c9	2020-04-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Dextrose and Electrolyte No. 48	SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, MONOBASIC POTASSIUM PHOSPHATE, SODIUM CHLORIDE AND DEXTROSE MONOHYDRATE	Baxter Healthcare Company	b283a454-0c20-4fbf-92d3-dae1f3cd3cad	2020-02-13	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	Baxter Healthcare Corporation	fbc01464-8885-4075-af41-911ffec5ae92	2020-01-27	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sterile Water	WATER	Baxter Healthcare Company	8bcf5572-49e1-4302-9522-56f57904cb4a	2019-12-29	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Renacidin	CITRIC ACID, GLUCONOLACTONE AND MAGNESIUM CARBONATE	United-Guardian, Inc.	13a9bbba-db21-4cba-991c-5d8afaf2ed74	2019-12-17	Warnings, Adverse reactions	Exact identifier unii: XF417D3PSL
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	e41adb4e-06fb-4141-ba55-50b043f3c9da	2019-11-19		Exact identifier unii: XF417D3PSL
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	14445dfd-6041-40cd-a043-3f4da6bcb9c1	2019-11-18		Exact identifier unii: XF417D3PSL
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	2557199a-5f60-49d8-b093-1e0700211243	2019-11-18		Exact identifier unii: XF417D3PSL
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	794f724c-87f0-49c1-9b26-c9e491978313	2019-11-18		Exact identifier unii: XF417D3PSL
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	5c7d3287-883a-459b-9214-074a583c8a59	2019-11-18		Exact identifier unii: XF417D3PSL
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	448a1dc5-7a98-4b2f-82af-4b92de05cfc3	2019-11-18		Exact identifier unii: XF417D3PSL
Plasma-Lyte A	SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE AND MAGNESIUM CHLORIDE	Baxter Healthcare Corporation	6ec9e61c-2c26-402f-8604-f446b2e34058	2019-08-05	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Potassium Chloride in Dextrose and Sodium Chloride	POTASSIUM CHLORIDE, DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE	Baxter Healthcare Company	c553fed1-3de5-4826-8eff-633b5923bf0b	2019-02-21	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
DermacinRx Lidotral	LIDOCAINE HYDROCHLORIDE	PureTek Corporation	23efec58-67cc-418d-85f5-7ef156443cbf	2019-02-04	Warnings, Adverse reactions	Exact identifier unii: V13007Z41A
Potassium Chloride in Sodium Chloride	POTASSIUM CHLORIDE AND SODIUM CHLORIDE	Baxter Healthcare Company	becc7410-0a25-49f5-b0c3-240078479dc8	2019-01-11	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Skin Klear Acne Relief	TRIBASIC CALCIUM PHOSPHATE, FUMARIA OFFICINALIS FLOWERING TOP, ARCTIUM LAPPA ROOT, SODIUM CHLORIDE, SAPONARIA OFFICINALIS ROOT, SILICON DIOXIDE, SOLIDAGO VIRGAUREA FLOWERING TOP, SULFUR, VIOLA TRICOLOR	Homeocare Laboratories	65afbc20-611b-4bc4-a151-c633bec66a82	2018-12-31	Warnings	Exact identifier unii: 451W47IQ8X
FREDS SALINE TWIN PACK LAXATIVE	SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM	FRED'S	7d15057f-eb3b-477f-ab14-68c3c38ea910	2018-12-26	Warnings	Exact identifier unii: GR686LBA74

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.