FDA.reportPublic FDA data

NDC 0010-6738 - Disal

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
0010-6738
Package NDCs from labels
0010-6738-01
Manufacturer
Boehringer Ingelheim Animal Health USA Inc.
Effective date
2025-04-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Disal® (furosemide tablets)Boehringer Ingelheim Animal Health USA Inc.2025-04-29PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0010-6738-01Disal500 in 1 BOTTLE, PLASTICTABLET5008

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0010-6738DISAL (FUROSEMIDE) TABLET [BOEHRINGER INGELHEIM ANIMAL HEALTH USA INC.]81 package rows20250430_e9c22b8d-81a4-4c4d-bb39-8f37256c5b7b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FUROSEMIDEACTIVE INGREDIENT7LXU5N7ZO5DISAL (FUROSEMIDE) TABLET [BOEHRINGER INGELHEIM VETMEDICA, INC.]1
FUROSEMIDEACTIVE MOIETY7LXU5N7ZO5DISAL (FUROSEMIDE) TABLET [BOEHRINGER INGELHEIM VETMEDICA, 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 8 of 8 · 152 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDEA-S Medication Solutions52f0c9d5-396f-4033-abe8-145eec3e69832023-02-06Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDELifestar Pharma LLC92f3ab5d-361c-4e12-bb50-fd4a9f195a8f2022-12-22Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProficient Rx LP595ddaf2-c2cb-44a4-a46c-53bcfe6bd7522022-12-01Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDESagent Pharmaceuticalsd63c1277-dd7e-4d21-9e80-68143f55e2dc2022-11-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDELeading Pharma, LLCb5c6fcf4-fd37-4fee-8dac-1a3273d95ffe2022-11-11Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPrecision Dose Inc.4a746634-379b-4847-a965-7607d2a71bed2022-09-21Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC6f124d7d-a19d-4de6-8ea4-719a42eb520b2022-03-10Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHF Acquisition Co LLC, DBA HealthFirstc5d9b063-e3fe-ec2f-e053-2995a90ab3f22021-06-28Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProficient Rx LPce84359c-2f76-421a-9b2b-79b1c2be2f202021-01-01Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEGland Pharma Limited644704c0-e6a5-4804-bfa6-795c8f83aa7a2020-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC1d2733ac-6fa6-44d1-96d4-f1a698045ad22018-04-18Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC6fbf7f3d-7566-44d5-9507-c4460238fc912018-02-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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