FDA.reportPublic FDA data

Doxycycline

Manufacturer
Blessings International
Effective date
2020-01-22
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:31:59

Label at a glance#

ProductDoxycycline
Active ingredientDoxycycline
Label structure1 sections

Label contents#

Full prescribing information#

PRINCIPAL DISPLAY PANEL - 100 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BLESSINGS
INTERNATIONAL®
MEDICINESFORMISSIONS

NDC 51376-780-10

Doxycycline

100 mg

1,000 Film Coated Tablets USP

RX ONLY / FOR EXPORT ONLY

PRINCIPAL DISPLAY PANEL - 100 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 100 mg Tablet Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1650142doxycycline monohydrate 100 MG Oral TabletPSN2
1650142doxycycline monohydrate 100 MG Oral TabletSCD2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DOXYCYCLINE ANHYDROUS Pharmacologic Class Indexing2Indexing - Pharmacologic Class20181113

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b4321c75-2e87-4d90-9726-9a28fb2293a3Product name320260112
5e99724e-0654-4aec-b7a2-0b9b10e312eeProduct name320250227
d2d36660-68ce-7e7d-0630-ec4b0d859fadProduct name620220921
a239f4dd-cf93-4660-b190-f97d000f249fProduct name720210607
a9d03566-caeb-4466-8021-74599b048880Product name320210604
12750814-20f7-4f35-b5fa-dbc8811ba858Product name920201007
00a5dbaa-1b7d-4e56-be0c-fedc7bbf5adeProduct name120200706
7b4b06ac-8c50-45f0-9556-293ea558a294Product name120180808
6a5b4392-5ab0-af0d-e0be-47b34e9dbb84Product name520171121
01a4aa74-7e05-63bd-bc10-1b5ceb111371Product name220171115
58b1278c-6dce-49b6-a05e-ea16f389acbaProduct name120160620

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51376-780-102022-01-28C16284748780-1d6a99b39-d3ed-a426-e053-dadaa90af4c2Doxycycline

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51376-780-10Doxycycline1000 in 1 BOTTLE, PLASTICTABLET, FILM COATED10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51376-780DOXYCYCLINE TABLET, FILM COATED [BLESSINGS INTERNATIONAL]21 package rows20200124_64448008-d16b-4527-81ec-85fcd6b6909d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51376-78051376-780-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
DoxycyclineN12000U13OACTIM
Magnesium Stearate70097M6I30IACT
Isopropyl AlcoholND2M416302IACT
Methylene Chloride588X2YUY0AIACT
Microcrystalline CelluloseOP1R32D61UIACT
Talc7SEV7J4R1UIACT
Starch, Potato8I089SAH3TIACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
dd1bb041-7b3a-4afc-9fb7-1d87ca19a59f64448008-d16b-4527-81ec-85fcd6b6909d2020-01-22Exact identifier
spl id: dd1bb041-7b3a-4afc-9fb7-1d87ca19a59f
spl set id: 64448008-d16b-4527-81ec-85fcd6b6909d

Reported adverse events (FAERS/openFDA)#

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