NDC 50102-120-01 - AUBRA

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
50102-120
Requested NDC
50102-120-01
Package NDCs from labels
50102-120-00, 50102-120-01, 50102-120-48, 50102-120-10, 50102-120-03
Manufacturer
Afaxys Pharma, LLC | Mylan Laboratories Limited
Effective date
2021-01-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
AUBRA - Afaxys Pharma, LLC | Mylan Laboratories LimitedAfaxys Pharma, LLC | Mylan Laboratories Limited2021-01-25HUMAN PRESCRIPTION DRUG LABEL
Aubra® (Levonorgestrel and Ethinyl Estradiol Tablets, USP 0.1 mg/0.02 mg)RPK Pharmaceuticals, Inc.2020-12-15HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50102-120-00EA - Each50102-120d9bee6d9-aa9d-4898-93de-438dae2bb86912022-06-06
50102-120-01EA - Each50102-1208b796782-496f-4ed0-b025-66127b0fc3f912013-11-04
50102-120-03EA - Each50102-120c2265cdf-ed8f-437d-9e4b-312af0119f7112017-09-11
50102-120-10EA - Each50102-1205c1fb698-e254-4b92-8ed9-eb87d360463212017-09-11
50102-120-48EA - Each50102-1208a66d499-33ea-4443-a859-d114a324025512013-11-04

DailyMed Socrata Ingredients#

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 8 of 9 · 171 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LevonorgestrelLEVONORGESTRELXiromed LLC626a2333-ff56-ef28-a287-b33bacc0302a2023-09-05WarningsExact identifier
unii: 5W7SIA7YZW
Household AntigensACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHURBioActive Nutritional3382df85-3ec5-4371-830e-4ed345b8f51b2023-07-14WarningsExact identifier
unii: 368GB5141J
PneumotoxTRITICUM AESTIVUM, ALFALFA, ARNICA MONTANA, ASCLEPIAS TUBEROSA, CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, FUCUS VESICULOSUS, HORDEUM VULGARE, IODIUM, NASTURTIUM AQUATICUM, PLANTAGO MAJOR, RAPHANUS SATIVUS, TRIFOLIUM PRATENSE, TRIGONELLA FOENUM-GRAECUM, SYMPHYTUM OFFICINALE, LUNG (SUIS), ORYZA SATIVA, SILICEA, ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ARSENICUM ALBUM, NATRUM MURIATICUM, NITRICUM ACIDUM,BioActive Nutritional, Inc.f8846fb1-92e5-4f8e-b3b3-bc620df90a622023-07-12WarningsExact identifier
unii: 368GB5141J
LILETTALEVONORGESTRELAllergan, Inc.aaf0eb2a-f88a-4f26-a445-0fd30176c3262023-06-29Warnings, Adverse reactionsExact identifier
unii: 5W7SIA7YZW
Ferrum OxydatumFERRUM OXYDATUMHahnemann Laboratories, INC.f8b52d3f-3fe2-a850-e053-6394a90a5d9f2023-04-06Exact identifier
unii: 1K09F3G675
LevonorgestrelLEVONORGESTRELNaari Pte Limitedbe8b7ace-9af8-4417-85fa-863e190728872023-03-16WarningsExact identifier
unii: 5W7SIA7YZW
09ac2d1c-97b5-4a05-af08-d58a0448c122efa6c9a7-ed87-4c86-ba37-534d551277552023-02-09Boxed warning, Warnings, Adverse reactionsExact identifier
spl set id: efa6c9a7-ed87-4c86-ba37-534d55127755
Next Choice One DoseLEVONORGESTRELFoundation Consumer Healthcare LLC504735bd-6af9-4588-bf85-d09dbf2a7e412023-02-02WarningsExact identifier
unii: 5W7SIA7YZW
Take ActionLEVONORGESTRELFoundation Consumer Healthcare LLC78eee7c9-5ca5-45af-898f-92a2f3b2598e2023-01-31WarningsExact identifier
unii: 5W7SIA7YZW
AfteraLEVONORGESTRELFoundation Consumer Healthcare LLC53ad8dff-9134-475c-90b3-8087753e17c42023-01-31WarningsExact identifier
unii: 5W7SIA7YZW
Plan B One-StepLEVONORGESTRELFoundation Consumer Healthcare LLC6ce6b40e-14ac-47bd-a648-ddf9e452e5592023-01-31WarningsExact identifier
unii: 5W7SIA7YZW
Opcicon One-StepLEVONORGESTRELSun Pharmaceutical Industries, Inc.b67ca313-561e-471f-baf3-257b7e253c752023-01-13WarningsExact identifier
unii: 5W7SIA7YZW
Petrochemical DetoxCHELIDONIUM MAJUS, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE, SYMPHYTUM OFFICINALE, ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ARSENICUM ALBUM, CADMIUM SULPHURATUM, GELSEMIUM SEMPERVIRENS, IRIDIUM METALLICUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PLATINUM METALLICUM, LATRODECTUS MACTANSDeseret Biologicals, Inc.b38b492a-cf45-4aa2-ba7e-4573d2c4ebe52023-01-12WarningsExact identifier
unii: 368GB5141J
Morning AfterLEVONORGESTRELRapha Pharmaceuticals, Inc.f0fab784-3d28-35fb-e053-2995a90ab6112022-12-29WarningsExact identifier
unii: 5W7SIA7YZW
Etonogestrel and Ethinyl EstradiolETONOGESTREL AND ETHINYL ESTRADIOLTeva Pharmaceuticals USA, Inc.a8cc104a-d522-49ad-af54-2f312b829b612022-09-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 423D2T571U
OptionelleLEVONORGESTREL TABLET, 1.5 MGStrides Pharma Inc1c7e849c-6392-48a6-9214-907325a012e22022-09-16WarningsExact identifier
unii: 5W7SIA7YZW
Levonorgestrel Tablet, 1.5 mgLEVONORGESTREL TABLET, 1.5 MGStrides Pharma Inc98f6367e-14d2-4c7a-9418-d996f0040d222022-09-13WarningsExact identifier
unii: 5W7SIA7YZW
My Choice TMLEVONORGESTRELProficient Rx LP165f7270-d050-4e97-b30f-107b96940d842022-09-01WarningsExact identifier
unii: 5W7SIA7YZW
LEVONORGESTREL AND ETHINYL ESTRADIOLLEVONORGESTREL AND ETHINYL ESTRADIOLMylan Pharmaceuticals Inc.c3c00dc0-8834-45fb-9f5b-810a98cef59d2022-08-31Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA200245
ZAFEMYNORELGESTROMIN AND ETHINYL ESTRADIOLAmneal Pharmaceuticals LLC5ee34c07-65af-42b8-a98f-e299ff90a8a12022-04-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 423D2T571U

Reported adverse events (FAERS/openFDA)#

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