NDC 69953-517 – Morning After

Levonorgestrel 1.5 mg/1.5mg · Tablet · Oral

Human Otc Drug

Product NDC69953-517

Product details

Brand name
Morning After
Generic name
Levonorgestrel
Labeler
Rapha Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205329
Marketed since
December 30, 2022
Listing expires
December 31, 2026
Pharmacologic class
Progestin; Progestin-containing Intrauterine Device

Active ingredients

Uses, dosage, side effects and warnings for Morning After →

Package NDC codes (1)

Package NDCDescriptionSince
69953-517-011 BLISTER PACK in 1 CARTON (69953-517-01) / 1 mg in 1 BLISTER PACKJan 16, 2023

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