NDC 58602-712

Fem Choice morning after

Levonorgestrel

Fem Choice morning after is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Aurohealth Llc. The primary component is Levonorgestrel.

Product ID58602-712_14051537-9d6c-4f73-a6e9-5eed554bbf65
NDC58602-712
Product TypeHuman Otc Drug
Proprietary NameFem Choice morning after
Generic NameLevonorgestrel
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-08
Marketing CategoryANDA /
Application NumberANDA206867
Labeler NameAurohealth LLC
Substance NameLEVONORGESTREL
Active Ingredient Strength2 mg/1
Pharm ClassesInhibit Ovum Fertilization [PE], Progesterone Congeners [CS], Progesterone Congeners [CS], Progestin [EPC], Progestin-containing Intrauterine Device [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 58602-712-28

1 BLISTER PACK in 1 CARTON (58602-712-28) > 1 TABLET in 1 BLISTER PACK
Marketing Start Date2015-12-08
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Fem Choice morning after" or generic name "Levonorgestrel"

NDCBrand NameGeneric Name
50102-111EContra EZlevonorgestrel
50102-211EContra One-StepLevonorgestrel
50419-424KyleenaLevonorgestrel
0536-1142LevonorgestrelLevonorgestrel
40032-620LevonorgestrelLevonorgestrel
40032-622LevonorgestrelLevonorgestrel
40051-054LEVONORGESTRELlevonorgestrel
49615-017LevonorgestrelLevonorgestrel
0023-5858LILETTALevonorgestrel
50419-423MirenaLevonorgestrel
43386-620My WayLevonorgestrel
43386-622My WayLevonorgestrel
16714-809New Daylevonorgestrel
21695-443NEXT CHOICELevonorgestrel
0113-2003Option 2levonorgestrel
21695-973Plan B One-Steplevonorgestrel
50090-1141Plan B One-StepLevonorgestrel
50090-3830Plan B One-Steplevonorgestrel
50090-5978Plan B One-Steplevonorgestrel
11509-0067Preventezalevonorgestrel
50419-422SkylaLevonorgestrel
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.