NDC 67046-135-03 - Doxycycline Hyclate

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
67046-135
Requested NDC
67046-135-03
Package NDCs from labels
67046-135-14, 67046-135-20, 67046-135-30, 67046-135-03
Manufacturer
Contract Pharmacy Services-PA
Effective date
2010-03-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Doxycycline Hyclate - Contract Pharmacy Services-PAContract Pharmacy Services-PA2010-03-10HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67046-135-142019-10-21C16284748780-1956f9ecf-d038-621f-e053-dbdaa90a74adDoxycycline Hyclate
67046-135-202019-10-21C16284748780-1956f9ecf-d038-621f-e053-dbdaa90a74adDoxycycline Hyclate
67046-135-302019-10-21C16284748780-1956f9ecf-d038-621f-e053-dbdaa90a74adDoxycycline Hyclate

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67046-135-14Doxycycline Hyclate14 in 1 BLISTER PACKCAPSULE141
67046-135-20Doxycycline Hyclate20 in 1 BLISTER PACKCAPSULE201
67046-135-30Doxycycline Hyclate30 in 1 BLISTER PACKCAPSULE301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67046-135DOXYCYCLINE HYCLATE CAPSULE [CONTRACT PHARMACY SERVICES-PA]1Legacy NDC, 3 package rows20100311_b34eb07b-d8a7-4762-a457-9d64dd86b205.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DOXYCYCLINE HYCLATEACTIVE INGREDIENT19XTS3T51UDOXYCYCLINE HYCLATE CAPSULE [CONTRACT PHARMACY SERVICES-PA]1
DOXYCYCLINE ANHYDROUSACTIVE MOIETY334895S862DOXYCYCLINE HYCLATE CAPSULE [CONTRACT PHARMACY SERVICES-PA]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UDOXYCYCLINE HYCLATE CAPSULE [CONTRACT PHARMACY SERVICES-PA]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XDOXYCYCLINE HYCLATE CAPSULE [CONTRACT PHARMACY SERVICES-PA]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30DOXYCYCLINE HYCLATE CAPSULE [CONTRACT PHARMACY SERVICES-PA]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 1 of 9 · 179 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Doxycycline HyclateDOXYCYCLINE HYCLATEREMEDYREPACK INC.051654c7-8ba6-44f2-842c-72f515e9b32d2026-09-15Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
doxycycline hyclateDOXYCYCLINE HYCLATEHAWAII REPACK, INC88c429a1-351d-432e-b69b-d7a0afca482a2026-09-09Warnings, Adverse reactionsExact identifier
rxcui: 1649988
unii: 19XTS3T51U
Doxycycline HyclateDOXYCYCLINE HYCLATEA-S Medication Solutions9ecadbc8-3087-4692-916a-b7f392d8e8da2026-09-09Warnings, Adverse reactionsExact identifier
application number: ANDA062396
unii: 19XTS3T51U
DOXYCYCLINE HYCLATEDOXYCYCLINE HYCLATEREMEDYREPACK INC.5fdc01c3-c62f-40cf-8351-91cbcc43d3792026-09-01Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
Doxycycline hyclateDOXYCYCLINE HYCLATEREMEDYREPACK INC.df44c686-de34-487a-8741-a0a12993cab22026-08-27Warnings, Adverse reactionsExact identifier
rxcui: 1649988
unii: 19XTS3T51U
DoxycyclineDOXYCYCLINE HYCLATEREMEDYREPACK INC.2c29f716-bdb0-437d-92a4-d856b87db9762026-08-26Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
DOXYCYCLINE HYCLATEDOXYCYCLINE HYCLATENuCare Pharmaceuticals,Inc.0106a3d3-db4d-f6ee-e063-6294a90a25e92026-08-26Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
DoxycyclineDOXYCYCLINE HYCLATEAcella Pharmaceuticals, LLC3fb9f5ad-90a2-4858-bc34-f800d8b2fa902026-08-18Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
doxycyclineDOXYCYCLINEREMEDYREPACK INC.f0fbf63a-e75c-40cf-b2e9-429deaac899d2026-08-10Warnings, Adverse reactionsExact identifier
rxcui: 1649988
unii: 19XTS3T51U
DoxycyclineDOXYCYCLINEAvenacy Inc.429813b4-0223-4d85-a844-b1227ff63b1e2026-08-06Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
Doxycycline HyclateDOXYCYCLINE HYCLATEMajor Pharmaceuticalse7c14a8e-c713-4f03-94e8-1ec9ae077d4d2026-08-05Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
Doxycycline HyclateDOXYCYCLINE HYCLATEREMEDYREPACK INC.2305ab4a-7d08-41f6-9c39-c9b6835be3892026-08-05Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
doxycyclineDOXYCYCLINEA-S Medication Solutionsfe8cd3c6-36d6-4d92-bc5c-833cd6f9cb322026-08-04Warnings, Adverse reactionsExact identifier
rxcui: 1649988
unii: 19XTS3T51U
DoxycyclineDOXYCYCLINE HYCLATEREMEDYREPACK INC.db53637e-16ac-41b0-b9d5-553471405d642026-08-03Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
DOXYCYCLINEDOXYCYCLINELupin Pharmaceuticals, Inc.2946fc05-78e5-4669-85d1-3a3979eceae02026-08-03Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
doxycyclineDOXYCYCLINEPreferred Pharmaceuticals Inc.bcc95094-80ed-4023-b2a6-955a4810bfbe2026-07-30Warnings, Adverse reactionsExact identifier
rxcui: 1649988
unii: 19XTS3T51U
Doxycycline HyclateDOXYCYCLINE HYCLATEPD-Rx Pharmaceuticals, Inc.cf95b2ca-2cf8-49a8-8e3a-f9b0f5b2072c2026-07-29Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
Doxycycline HyclateDOXYCYCLINE HYCLATEPD-Rx Pharmaceuticals, Inc.3af9348c-a98b-4059-a5ef-4229e2b33af02026-07-20Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
Doxycycline HyclateDOXYCYCLINE HYCLATEPD-Rx Pharmaceuticals, Inc.0994d23a-f9e4-4c33-ba44-a1f4ae4a312c2026-07-20Warnings, Adverse reactionsExact identifier
rxcui: 1649988
unii: 19XTS3T51U
Doxycycline HyclateDOXYCYCLINE HYCLATEPD-Rx Pharmaceuticals, Inc.1401d590-0967-4c6b-b52b-a83e9f6df0972026-07-17Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U

Reported adverse events (FAERS/openFDA)#

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