FDA.reportPublic FDA data

NDC 70518-3488-01 - doxycycline

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
70518-3488
Requested NDC
70518-3488-01
Package NDCs from labels
70518-3488-0, 70518-3488-1, 70518-3488-2, 70518-3488-3, 70518-3488-4, 70518-3488-5, 70518-3488-6, 70518-3488-7, 70518-3488-8, 70518-3488-9, 70518-3488-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-08-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
doxycycline hyclate capsulesREMEDYREPACK INC.2026-08-10HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-3488-0doxycycline20 in 1 BLISTER PACKCAPSULE2018
70518-3488-1doxycycline30 in 1 BLISTER PACKCAPSULE3018
70518-3488-2doxycycline14 in 1 BOTTLE, PLASTICCAPSULE1418
70518-3488-3doxycycline28 in 1 BOTTLE, PLASTICCAPSULE2818
70518-3488-4doxycycline20 in 1 BOTTLE, PLASTICCAPSULE2018
70518-3488-5doxycycline180 in 1 BOTTLE, PLASTICCAPSULE18018
70518-3488-6doxycycline56 in 1 BOTTLE, PLASTICCAPSULE5618
70518-3488-7doxycycline30 in 1 BOTTLE, PLASTICCAPSULE3018
70518-3488-8doxycycline50 in 1 BOTTLE, PLASTICCAPSULE5018
70518-3488-9doxycycline20 in 1 BOTTLE, PLASTICCAPSULE2018

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-3488DOXYCYCLINE CAPSULE [REMEDYREPACK INC.]11Current NDC, Legacy NDC, 10 package rows20250418_f0fbf63a-e75c-40cf-b2e9-429deaac899d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70518-3488-4EA - Each70518-34880fb9e860-0324-4d69-b258-32a9b5e06b0412026-01-08

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 2 of 113 · 2,252 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Protect Tinted Mineral SunscreenBROAD SPECTRUM SPF30Opal Day Spa5943413a-48e1-0bdf-e063-6294a90a2fff2026-08-17WarningsExact identifier
unii: 15FIX9V2JP
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30MedSpa By Beauty Bar LLC5943ba3d-688e-9e9c-e063-6294a90afa9a2026-08-17WarningsExact identifier
unii: 15FIX9V2JP
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30CORBY, JR., TERRY L.594443fd-8e27-4ec6-e063-6294a90a3ff02026-08-17WarningsExact identifier
unii: 15FIX9V2JP
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30DR. SAMRAO'S OFFICE58b2ca35-11ed-d848-e063-6294a90a5b372026-08-11WarningsExact identifier
unii: 15FIX9V2JP
doxycyclineDOXYCYCLINEREMEDYREPACK INC.f0fbf63a-e75c-40cf-b2e9-429deaac899d2026-08-10Warnings, Adverse reactionsExact identifier
application number: ANDA209402
ndc (package): 70518-3488-1
ndc (package): 70518-3488-4
ndc (package): 70518-3488-5
ndc (package): 70518-3488-6
ndc (package): 70518-3488-8
ndc (package): 70518-3488-3
ndc (package): 70518-3488-2
ndc (package): 70518-3488-0
ndc (package): 70518-3488-7
ndc (package): 70518-3488-9
ndc (product): 70518-3488
ndc11 (package): 70518348801
rxcui: 1649988
spl id: 58b75f14-35b1-fd4c-e063-6394a90aefc7
spl set id: f0fbf63a-e75c-40cf-b2e9-429deaac899d
unii: 19XTS3T51U
Journee Firm Riche Broad Spectrum Sunscreen SPF 30TITANIUM DIOXIDE AND ZINC OXIDEMerz North America, Inc.d4d4bfcf-3674-4847-8ad8-1716a8e821ae2026-08-10WarningsExact identifier
unii: 15FIX9V2JP
VEIRFOO Brightening Hydrating Antiwrinkle SunscreenTITANIUM DIOXIDE, OCTINOXATELCM TECHNOLOGY Co., Ltd4cbbf8aa-8910-b7e7-e063-6294a90a4f072026-08-07WarningsExact identifier
unii: 15FIX9V2JP
DoxycyclineDOXYCYCLINEAvenacy Inc.429813b4-0223-4d85-a844-b1227ff63b1e2026-08-06Warnings, Adverse reactionsExact identifier
unii: 19XTS3T51U
CalamineFERRIC OXIDE REDThe Kroger Co.9ddcd6ba-1aed-48f8-a91a-54bd6f0d93082026-08-06Warnings, Adverse reactionsExact identifier
unii: 1K09F3G675
EltaMD UV RestoreTITANIUM DIOXIDE, ZINC OXIDE SUNSCREENCP Skin Health Group, Inc37fee381-ce6b-4949-9a4a-778aa839fb842026-08-06WarningsExact identifier
unii: 15FIX9V2JP
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
application number: ANDA209402
rxcui: 1649988
unii: 19XTS3T51U
Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEYOCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8%Lale Cosmetics LLC581fb0cd-c55d-d562-e063-6394a90a7f112026-08-03WarningsExact identifier
unii: 15FIX9V2JP
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
EltaMD UV ActiveZINC OXIDE AND TITANIUM DIOXIDE SUNSCREENCP Skin Health Group, Inc39d16479-d491-4c19-aa11-674461687c7b2026-08-03WarningsExact identifier
unii: 15FIX9V2JP
Continuous Correction CreamTITANIUM DIOXIDEBaxter of California, LLC1cbcc648-f2e1-af60-e063-6294a90ad4bb2026-07-31WarningsExact identifier
unii: 15FIX9V2JP
Cover CremeTITANIUM DIOXIDEBaxter of California31f5e8c4-523f-4596-e063-6294a90a6a122026-07-31WarningsExact identifier
unii: 15FIX9V2JP
doxycyclineDOXYCYCLINEPreferred Pharmaceuticals Inc.bcc95094-80ed-4023-b2a6-955a4810bfbe2026-07-30Warnings, Adverse reactionsExact identifier
application number: ANDA209402
rxcui: 1649988
unii: 19XTS3T51U

Reported adverse events (FAERS/openFDA)#

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