MICROGESTIN Fe 1/20

Product NDC: 51862-012
11-digit product format: 518620012
Labeler code: 51862
Product ID: 51862-012_61aaa6fc-82d4-47cb-bfb5-0d2cc855340b
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: norethindrone acetate and ethinyl estradiol and ferrous fumarate
Dosage form: KIT
Labeler: Mayne Pharma Inc.
Application: NDA017354
Marketing category: NDA AUTHORIZED GENERIC
Marketing start: 2016-08-05
Marketing end: 2022-10-31
Active strength: 0
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 NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51862-012-01	EA - Each	51862-012	3281795b-84ef-4ca1-8c0a-65c1046d83fb	1	2017-03-06
51862-012-06	EA - Each	51862-012	d3014992-3297-43f0-8ae2-948667ab3def	1	2016-12-07

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
51862-012-06	51862001206	6 BLISTER PACK in 1 CARTON (51862-012-06) > 1 KIT in 1 BLISTER PACK	6 blister pack	2016-08-05	0000-00-00	No	No	Current