FDA.reportPublic FDA data

NDC 70710-1710-01 - ketorolac tromethamine

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
70710-1710
Requested NDC
70710-1710-01
Package NDCs from labels
70710-1710-1, 70710-1710-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-08-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ketorolac Tromethamine Tablets USP, 10 mg Rx onlyREMEDYREPACK INC.2026-08-06HUMAN PRESCRIPTION DRUG LABEL
Ketorolac Tromethamine Tablets USP, 10 mg Rx onlyPreferred Pharmaceuticals Inc.2026-06-10HUMAN PRESCRIPTION DRUG LABEL
ketorolac tromethamine - Redpharm DrugRedpharm Drug2026-05-15HUMAN PRESCRIPTION DRUG LABEL
ketorolac tromethamine - Bryant Ranch PrepackBryant Ranch Prepack2026-02-16HUMAN PRESCRIPTION DRUG LABEL
ketorolac tromethamine - A-S Medication SolutionsA-S Medication Solutions2025-12-04HUMAN PRESCRIPTION DRUG LABEL
Ketorolac Tromethamine Tablets USP, 10 mg Rx onlyNuCare Pharmaceuticals,Inc.2025-04-25HUMAN PRESCRIPTION DRUG LABEL
Ketorolac Tromethamine Tablets USP, 10 mg Rx onlyZydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Global FZE | Zydus Lifesciences Limited2024-08-06HUMAN PRESCRIPTION DRUG LABEL
Ketorolac Tromethamine Tablets USP, 10 mg Rx onlyNuCare Pharmaceuticals,Inc.2024-04-05HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70710-1710-1ketorolac tromethamine100 in 1 BOTTLETABLET, FILM COATED1005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70710-1710KETOROLAC TROMETHAMINE TABLET, FILM COATED [ZYDUS PHARMACEUTICALS (USA) INC.]5Current NDC, Legacy NDC, 1 package rows20240807_ffd84ef3-26ed-4810-952b-4f0e913c5e32.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70710-1710-1EA - Each70710-17101b615fbc-f337-4f20-8035-df5ee7f226ad12023-02-06

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 107 of 107 · 2,124 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Meijer Baby Tear Free SPF 50TITANIUM DIOXIDE, ZINC OXIDEMeijer Distributing Inc.2434de23-bcc9-4a83-9945-16fc3f2b8c612016-06-01WarningsExact identifier
unii: 15FIX9V2JP
TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted)OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDEAllergan, Inc.6a996e03-907f-4e6a-b232-0892b86956b02015-08-21WarningsExact identifier
unii: 15FIX9V2JP
Renewal Firming Day Broad Spectrum SPF 30TITANIUM DIOXIDE, ZINC OXIDEBURT'S BEES, INC.18ceb5d8-4b76-6a54-e054-00144ff88e882015-06-18WarningsExact identifier
unii: 15FIX9V2JP
TiZO2TITANIUM DIOXIDE, ZINC OXIDEFallien Cosmeceuticals, LTD.30468afc-9616-4765-b046-12e97a0a78272010-12-20WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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