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Product NDC
51862-100
11-digit product format
518620100
Labeler code
51862
Product ID
51862-100_05c452d3-dfac-4036-8c2d-536a03ed99a0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Norethindrone
Dosage form
TABLET
Route
ORAL
Labeler
Mayne Pharma Inc.
Application
ANDA076225
Marketing category
ANDA
Marketing start
2016-08-03
Marketing end
2020-04-30
Substance
NORETHINDRONE
Active strength
0 mg/1
Pharmacologic classes
Progesterone Congeners [CS],Progestin [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51862-100-01EA - Each51862-1008bf50645-c5e8-4421-959e-00ea2c9f56ea12017-03-06
51862-100-06EA - Each51862-100744b31fc-17a0-46ef-941d-73ec3005d72412017-03-06