morning after

Generic: levonorgestrel

Labeler: rapha pharmaceuticals, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name morning after
Generic Name levonorgestrel
Labeler rapha pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levonorgestrel 1.5 mg/1.5mg

Manufacturer
Rapha Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 69953-515
Product ID 69953-515_677aa953-3c31-4ce5-e053-2991aa0ab2b2
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206867
Listing Expiration 2026-12-31
Marketing Start 2018-03-22

Pharmacologic Class

Established (EPC)
progestin [epc] progestin-containing intrauterine system [epc]
Chemical Structure
progesterone congeners [cs]
Physiologic Effect
inhibit ovum fertilization [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69953515
Hyphenated Format 69953-515

Supplemental Identifiers

RxCUI
483325 1657617
UPC
0369953515017
UNII
5W7SIA7YZW
NUI
N0000175830 M0447349 N0000175602 N0000175832

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name morning after (source: ndc)
Generic Name levonorgestrel (source: ndc)
Application Number ANDA206867 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 mg/1.5mg
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (69953-515-01) / 1 mg in 1 BLISTER PACK
source: ndc

Packages (1)

69953-515-01 1 BLISTER PACK in 1 CARTON (69953-515-01) / 1 mg in 1 BLISTER PACK

Ingredients (1)

levonorgestrel (1.5 mg/1.5mg)

Linked Drug Pages (1)

Morning After ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "677aa953-3c31-4ce5-e053-2991aa0ab2b2", "openfda": {"nui": ["N0000175830", "M0447349", "N0000175602", "N0000175832"], "upc": ["0369953515017"], "unii": ["5W7SIA7YZW"], "rxcui": ["483325", "1657617"], "spl_set_id": ["677aa953-3c30-4ce5-e053-2991aa0ab2b2"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_pe": ["Inhibit Ovum Fertilization [PE]"], "pharm_class_epc": ["Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "manufacturer_name": ["Rapha Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69953-515-01)  / 1 mg in 1 BLISTER PACK", "package_ndc": "69953-515-01", "marketing_start_date": "20180322"}], "brand_name": "Morning After", "product_id": "69953-515_677aa953-3c31-4ce5-e053-2991aa0ab2b2", "dosage_form": "TABLET", "pharm_class": ["Inhibit Ovum Fertilization [PE]", "Progesterone Congeners [CS]", "Progesterone Congeners [CS]", "Progestin [EPC]", "Progestin-containing Intrauterine Device [EPC]"], "product_ndc": "69953-515", "generic_name": "Levonorgestrel", "labeler_name": "Rapha Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Morning After", "active_ingredients": [{"name": "LEVONORGESTREL", "strength": "1.5 mg/1.5mg"}], "application_number": "ANDA206867", "marketing_category": "ANDA", "marketing_start_date": "20180322", "listing_expiration_date": "20261231"}