emergency contraceptive

Generic: levonorgestrel

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name emergency contraceptive
Generic Name levonorgestrel
Labeler p & l development, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levonorgestrel 1.5 mg/1

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-138
Product ID 59726-138_a54c8af1-220b-4fb8-bfea-59ae42870c19
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA205329
Listing Expiration 2026-12-31
Marketing Start 2023-08-01

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 59726138
Hyphenated Format 59726-138

Supplemental Identifiers

RxCUI
483325
UPC
0359726138017
UNII
5W7SIA7YZW
NUI
N0000175830 M0447349 N0000175602 N0000175832

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 emergency contraceptive (source: ndc)
Generic Name levonorgestrel (source: ndc)
Application Number ANDA205329 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (59726-138-01) / 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": "a54c8af1-220b-4fb8-bfea-59ae42870c19", "openfda": {"nui": ["N0000175830", "M0447349", "N0000175602", "N0000175832"], "upc": ["0359726138017"], "unii": ["5W7SIA7YZW"], "rxcui": ["483325"], "spl_set_id": ["25676fc2-1f1f-40d2-8e84-3e52c8abda49"], "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": ["P & L Development, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (59726-138-01)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "59726-138-01", "marketing_start_date": "20230801"}], "brand_name": "Emergency Contraceptive", "product_id": "59726-138_a54c8af1-220b-4fb8-bfea-59ae42870c19", "dosage_form": "TABLET", "pharm_class": ["Inhibit Ovum Fertilization [PE]", "Progesterone Congeners [CS]", "Progesterone Congeners [CS]", "Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "product_ndc": "59726-138", "generic_name": "Levonorgestrel", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Emergency Contraceptive", "active_ingredients": [{"name": "LEVONORGESTREL", "strength": "1.5 mg/1"}], "application_number": "ANDA205329", "marketing_category": "ANDA", "marketing_start_date": "20230801", "listing_expiration_date": "20261231"}