NDC 51862-866

Microgestin Fe 1/20

Norethindrone Acetate/ethinyl Estradiol And Ferrous Fumarate

Microgestin Fe 1/20 is a Kit in the Human Prescription Drug category. It is labeled and distributed by Mayne Pharma Inc.. The primary component is .

Product ID51862-866_7fe013d6-bb93-41df-8110-33d210eeab1f
NDC51862-866
Product TypeHuman Prescription Drug
Proprietary NameMicrogestin Fe 1/20
Generic NameNorethindrone Acetate/ethinyl Estradiol And Ferrous Fumarate
Dosage FormKit
Marketing Start Date2020-10-12
Marketing CategoryANDA / ANDA
Application NumberANDA091454
Labeler NameMayne Pharma Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 51862-866-01

1 BLISTER PACK in 1 PACKET (51862-866-01) > 1 KIT in 1 BLISTER PACK
Marketing Start Date2020-10-12
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Microgestin Fe 1/20" or generic name "Norethindrone Acetate/ethinyl Estradiol And Ferrous Fumarate"

NDCBrand NameGeneric Name
51862-012MICROGESTIN Fe 1/20norethindrone acetate and ethinyl estradiol and ferrous fumarate
51862-866Microgestin Fe 1/20Norethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate
53002-1616MICROGESTIN Fe 1/20norethindrone acetate and ethinyl estradiol and ferrous fumarate
53002-2616Microgestin Fe 1/20Norethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate
16714-416Larin 24 FeNorethindrone acetate/Ethinyl Estradiol and Ferrous Fumarate
16714-405Larin Fe 1.5/30Norethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate
50090-2559Larin Fe 1.5/30Norethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate
16714-406Larin Fe 1/20Norethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate
50090-2511Larin Fe 1/20Norethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate
51862-648Microgestin 24 FeNorethindrone acetate/Ethinyl Estradiol and Ferrous Fumarate
51862-870Microgestin Fe 1.5/30Norethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.