NDC 70518-1385-01 - venlafaxine

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
70518-1385
Requested NDC
70518-1385-01
Package NDCs from labels
70518-1385-0, 70518-1385-1, 70518-1385-2, 70518-1385-3, 70518-1385-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-07-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Venlafaxine Tablets, USP Rx onlyREMEDYREPACK INC.2026-07-06HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-1385-0venlafaxine30 in 1 BLISTER PACKTABLET3018
70518-1385-1venlafaxine90 in 1 BOTTLE, PLASTICTABLET9018
70518-1385-2venlafaxine30 in 1 BOTTLE, PLASTICTABLET3018
70518-1385-3venlafaxine60 in 1 BOTTLE, PLASTICTABLET6018

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-1385VENLAFAXINE (VENLAFAXINE HYDROCHLORIDE) TABLET [REMEDYREPACK INC.]14Current NDC, Legacy NDC, 4 package rows20250223_4a82cef5-693e-46e9-90c4-bff753cdce37.zip

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 3 of 39 · 780 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Venlafaxine HydrochlorideVENLAFAXINE HYDROCHLORIDEPURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALSb1d21366-f686-4e20-a10f-0c25f517db382026-07-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7D7RX5A8MO
venlafaxineVENLAFAXINE HYDROCHLORIDEREMEDYREPACK INC.f56a0f70-bbb1-4e69-b969-965a72f0e2f02026-07-28Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA090555
rxcui: 313586
unii: 7D7RX5A8MO
PridICHTHAMMOL, CALCIUM SULFIDE, CALENDULA OFFICINALIS FLOWERING TOP, ARNICA MONTANA, ECHINACEA ANGUSTIFOLIA, SILICON DIOXIDE, SULFURHyland's Inc.49689eeb-7790-07f1-e063-6294a90a2df22026-07-16WarningsExact identifier
unii: ETJ7Z6XBU4
Leg Cramps PMOYSTER SHELL CALCIUM CARBONATE, CRUDE, CAUSTICUM, MATRICARIA RECUTITA, CINCHONA OFFICINALIS BARK, COPPER, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, AND SULFURHyland's Inc.b0574a7e-88fa-417e-b6d5-60ced59eba472026-07-15WarningsExact identifier
unii: ETJ7Z6XBU4
Jacksons Cell Salts SILICA 12X 12SILICEAZettl Health Inc.5647dafc-1fff-6a25-e063-6294a90a8b4f2026-07-10Exact identifier
unii: ETJ7Z6XBU4
Venlafaxine HydrochlorideVENLAFAXINE HYDROCHLORIDEREMEDYREPACK INC.4e3053b9-cdec-4f4d-85ae-2e55cf1cc1852026-07-08Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7D7RX5A8MO
Venlafaxine HydrochlorideVENLAFAXINE HYDROCHLORIDEREMEDYREPACK INC.50d3b487-9f65-4e2f-b6eb-9533964f89722026-07-08Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7D7RX5A8MO
Venlafaxine HydrochlorideVENLAFAXINE HYDROCHLORIDEREMEDYREPACK INC.ac9b972d-8b8a-4727-90c2-b208f91272fd2026-07-08Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7D7RX5A8MO
Venlafaxine HydrochlorideVENLAFAXINE HYDROCHLORIDEYaopharma Co., Ltd.38fd2c97-cd30-2f7d-e054-00144ff8d46c2026-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 314277
rxcui: 313586
rxcui: 313582
rxcui: 313584
rxcui: 313580
unii: 7D7RX5A8MO
venlafaxineVENLAFAXINE HYDROCHLORIDEREMEDYREPACK INC.4a82cef5-693e-46e9-90c4-bff753cdce372026-07-06Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA090555
ndc (package): 70518-1385-1
ndc (package): 70518-1385-0
ndc (package): 70518-1385-3
ndc (package): 70518-1385-2
ndc (product): 70518-1385
ndc11 (package): 70518138501
rxcui: 313584
spl id: 55f229f7-3af4-e3d8-e063-6394a90a8dc9
spl set id: 4a82cef5-693e-46e9-90c4-bff753cdce37
unii: 7D7RX5A8MO
Venlafaxine HydrochlorideVENLAFAXINE HYDROCHLORIDEA-S Medication Solutionsf50029b8-7d05-445a-9d9f-71a1aee6088b2026-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7D7RX5A8MO
The Cell Salt Co. Daily Blend 12 in 1CALC FLUOR, CALC PHOS, CALC SULPH, FERRUM PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT MUR, NAT PHOS, NAT SULPH, SILICEAThe Cell Salt Company LLC55826f59-acf4-7370-e063-6394a90afed72026-07-01WarningsExact identifier
unii: ETJ7Z6XBU4
Venlafaxine HydrochlorideVENLAFAXINE HYDROCHLORIDEA-S Medication Solutions5a990dbd-f280-4caf-b950-4703ee98b2302026-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7D7RX5A8MO
Venlafaxine HydrochlorideVENLAFAXINE HYDROCHLORIDEA-S Medication Solutionsd94e5404-f728-4e4b-af99-8a8e4dfae2272026-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7D7RX5A8MO
Venlafaxine HydrochlorideVENLAFAXINE HYDROCHLORIDEA-S Medication Solutionsc37a73fa-ceee-4555-a61b-e1e66ad6e97d2026-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7D7RX5A8MO
Bambusa StannumBAMBUSA STANNUMUriel Pharmacy Inc.a0d4d0ac-e2d2-4381-8f93-e417195218592026-06-30WarningsExact identifier
unii: ETJ7Z6XBU4
VenlafaxineVENLAFAXINESt. Mary's Medical Park Pharmacyfab65158-b2f7-1db7-e053-6294a90af2312026-06-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 313584
unii: 7D7RX5A8MO
VENLAFAXINEVENLAFAXINEHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.80ac757d-c629-4579-8afd-cae0ee9cd6142026-06-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 314277
rxcui: 313586
rxcui: 313582
rxcui: 313584
rxcui: 313580
unii: 7D7RX5A8MO
H-Scars FormulaCALENDULA OFFICINALLIS, SILICEAHealing Natural Oils LLC8433ff00-d815-45e0-b0ec-1448668dd8f82026-06-16WarningsExact identifier
unii: ETJ7Z6XBU4
E-Z-GAS IIANTACID/ANTIFLATULENTE-Z-EM, INC.4e12e1cb-b033-076d-e054-00144ff8d46c2026-06-15WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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