NDC 51862-102-01 - Camila

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
51862-102
Requested NDC
51862-102-01
Package NDCs from labels
51862-102-01, 51862-102-06
Manufacturer
Mayne Pharma Inc. | Teva Pharmaceuticals USA, Inc.
Effective date
2018-10-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Camila ® (norethindrone tablets USP, 0.35 mg)Mayne Pharma Inc. | Teva Pharmaceuticals USA, Inc.2018-10-17HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51862-102-01EA - Each51862-102654cd1b0-0377-4425-92e8-4b83fab15ef612017-05-03
51862-102-06EA - Each51862-102b918672e-15bc-4b3d-804d-36718689756112016-09-02

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 2 · 24 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IncassiaNORETHINDRONEAurobindo Pharma Limited0b87cef0-610c-469d-92ba-4007f4bc38782021-09-14Warnings, Adverse reactionsExact identifier
unii: T18F433X4S
NorethindroneNORETHINDRONEProficient Rx LPfb84b86e-5f1f-4c17-8b69-ff695c5faf552019-11-01Warnings, Adverse reactionsExact identifier
unii: T18F433X4S
NORETHINDRONENORETHINDRONEMylan Pharmaceuticals Inc.af851d82-b30f-463b-9dba-0437225dc1ee2018-10-23Boxed warning, Warnings, Adverse reactionsExact identifier
unii: T18F433X4S
4e7d704c-562d-4b01-b700-931fd28b68cb8cedd2ff-473d-4a8e-87d1-9758cc19238a2018-10-17Warnings, Adverse reactionsExact identifier
spl id: 4e7d704c-562d-4b01-b700-931fd28b68cb
spl set id: 8cedd2ff-473d-4a8e-87d1-9758cc19238a

Reported adverse events (FAERS/openFDA)#

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