EContra EZ

Product NDC: 50102-111
11-digit product format: 501020111
Labeler code: 50102
Product ID: 50102-111_fdcd4d53-36e0-4c33-933f-e2e2194a919a
Type: HUMAN OTC DRUG
Nonproprietary name: levonorgestrel
Dosage form: TABLET
Route: ORAL
Labeler: Afaxys Pharma, LLC
Application: ANDA202739
Marketing category: ANDA
Marketing start: 2015-01-01
Marketing end: 0000-00-00
Substance: LEVONORGESTREL
Active strength: 2 mg/1
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50102-111-12	2023-04-26	C162847	48780-1	d6a99b39-d3af-a426-e053-dadaa90af4c2	5752210e-459b-467c-8fda-b5976c07d88e
50102-111-12	2022-01-28	C162847	48780-1	d6a99b39-d3af-a426-e053-dadaa90af4c2	5752210e-459b-467c-8fda-b5976c07d88e

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50102-111-01	EA - Each	50102-111	874f3fb8-07bf-4f88-98f8-305d46e18d29	1	2015-03-03
50102-111-12	EA - Each	50102-111	b0a383b1-eb41-46d0-b404-749a16f30277	1	2015-03-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
50102-111-12	50102011112	12 CARTON in 1 PACKAGE (50102-111-12) > 1 BLISTER PACK in 1 CARTON (50102-111-01) > 1 TABLET in 1 BLISTER PACK (50102-111-00)	12 carton	2015-01-01	0000-00-00	No	No	Current