NDC 58151-237-32 - Lyrica

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
58151-237
Requested NDC
58151-237-32
Package NDCs from labels
58151-237-32, 58151-237-88, 58151-237-77
Manufacturer
Viatris Specialty LLC
Effective date
2025-04-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lyrica - Viatris Specialty LLCViatris Specialty LLC2025-04-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58151-237-32Lyrica1 in 1 BLISTER PACKCAPSULE118
58151-237-77Lyrica90 in 1 BOTTLECAPSULE9018
58151-237-88Lyrica100 in 1 CARTONCAPSULE10018

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58151-237LYRICA (PREGABALIN) CAPSULE LYRICA (PREGABALIN) SOLUTION [VIATRIS SPECIALTY LLC]11Current NDC, 3 package rows20250510_d4734e7d-5079-455e-8ff5-8f4539c998a9.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
58151-237-32EA - Each58151-23781f7ce3e-307b-4aef-82be-a1a737ebaf0212024-12-10
58151-237-77EA - Each58151-2375bb79087-c214-4f9d-a82e-e98e8c0fbe9412024-12-10
58151-237-88EA - Each58151-2378dd7f9cd-607f-48f4-91b3-6a6962d9899112024-12-10

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 156 of 156 · 3,103 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
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.