morning after pill

Generic: levonorgestrel

Labeler: cadence health inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name morning after pill
Generic Name levonorgestrel
Labeler cadence health inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levonorgestrel 1.5 mg/1

Manufacturer
Cadence Health Inc

Identifiers & Regulatory

Product NDC 73436-8292
Product ID 73436-8292_32e9d9ba-b359-4826-e063-6294a90a927b
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207660
Listing Expiration 2026-12-31
Marketing Start 2025-04-15

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 734368292
Hyphenated Format 73436-8292

Supplemental Identifiers

RxCUI
483325 1657617
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 pill (source: ndc)
Generic Name levonorgestrel (source: ndc)
Application Number ANDA207660 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 BOX, UNIT-DOSE (73436-8292-1) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

levonorgestrel (1.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32e9d9ba-b359-4826-e063-6294a90a927b", "openfda": {"nui": ["N0000175830", "M0447349", "N0000175602", "N0000175832"], "unii": ["5W7SIA7YZW"], "rxcui": ["483325", "1657617"], "spl_set_id": ["2fb59f53-d885-9d4a-e063-6394a90a88cc"], "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": ["Cadence Health Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 BOX, UNIT-DOSE (73436-8292-1)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "73436-8292-1", "marketing_start_date": "20250415"}], "brand_name": "Morning After Pill", "product_id": "73436-8292_32e9d9ba-b359-4826-e063-6294a90a927b", "dosage_form": "TABLET", "pharm_class": ["Inhibit Ovum Fertilization [PE]", "Progesterone Congeners [CS]", "Progesterone Congeners [CS]", "Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "product_ndc": "73436-8292", "generic_name": "levonorgestrel", "labeler_name": "Cadence Health Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Morning After Pill", "active_ingredients": [{"name": "LEVONORGESTREL", "strength": "1.5 mg/1"}], "application_number": "ANDA207660", "marketing_category": "ANDA", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}