postday one-step

Generic: levonorgestrel

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

Drug Facts

Product Profile

Brand Name postday one-step
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 69953-618
Product ID 69953-618_0aab0d9b-3db7-7c71-e063-6394a90a9c89
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA205329
Listing Expiration 2026-12-31
Marketing Start 2023-11-21

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 69953618
Hyphenated Format 69953-618

Supplemental Identifiers

RxCUI
483325 2049247
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 postday one-step (source: ndc)
Generic Name levonorgestrel (source: ndc)
Application Number ANDA205329 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 mg/1.5mg
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (69953-618-43) / 1 mg in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

levonorgestrel (1.5 mg/1.5mg)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0aab0d9b-3db7-7c71-e063-6394a90a9c89", "openfda": {"nui": ["N0000175830", "M0447349", "N0000175602", "N0000175832"], "unii": ["5W7SIA7YZW"], "rxcui": ["483325", "2049247"], "spl_set_id": ["6f7f5697-acb6-ea95-e053-2991aa0ae7c7"], "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 (69953-618-43)  / 1 mg in 1 BLISTER PACK", "package_ndc": "69953-618-43", "marketing_start_date": "20231121"}], "brand_name": "PostDay One-Step", "product_id": "69953-618_0aab0d9b-3db7-7c71-e063-6394a90a9c89", "dosage_form": "TABLET", "pharm_class": ["Inhibit Ovum Fertilization [PE]", "Progesterone Congeners [CS]", "Progesterone Congeners [CS]", "Progestin [EPC]", "Progestin-containing Intrauterine System [EPC]"], "product_ndc": "69953-618", "generic_name": "Levonorgestrel", "labeler_name": "Rapha Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PostDay One-Step", "active_ingredients": [{"name": "LEVONORGESTREL", "strength": "1.5 mg/1.5mg"}], "application_number": "ANDA205329", "marketing_category": "ANDA", "marketing_start_date": "20231121", "listing_expiration_date": "20261231"}