58602-712 : Fem Choice Morning After 1.5 mg Oral Tablet


NDC: 58602-712
Labeler: Aurohealth LLC
Product Type: Human OTC Drug
Drug Name:  Fem Choice Morning After
Dosage Form: Oral Tablet
Application #: ANDA206867
Rev. Date: 


NDC Package Codes:

  • 58602-712-28: 1 BLISTER PACK IN 1 CARTON (58602‑712‑28) > 1 TABLET IN 1 BLISTER PACK

Active Ingredients:

  • Levonorgestrel

Dosage Strength:

  • 1.5 mg

Pharmaceutical Classes:

  • Inhibit Ovum Fertilization [PE]
  • Progesterone Congeners [CS]
  • Progestin [EPC]
  • Progestin-containing Intrauterine Device [EPC]

Related Products:

Based on records with the same trade name.
  • 58602-891 Fem Choice Morning After 1.5 mg Oral Tablet by Aurohealth LLC

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.