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Levonorgestrel 1.5 MG Oral Tablet [PostDay One-Step] — RxCUI 2049247

RxNorm drug concept · Semantic branded drug
RxCUI 2049247 Semantic branded drug · SBD ● Current RxNorm concept 4 FDA products 4 package NDCs Snapshot Jul 14, 2026

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Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.

🗂️ Key Facts

RxCUI2049247
Official nameLevonorgestrel 1.5 MG Oral Tablet [PostDay One-Step]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asPostDay One-Step 1.5 MG Oral Tablet; PostDay One-Step Emergency Contraceptive 1.5 MG Oral Tablet
FDA products mapped4
Package NDCs mapped4
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

Our pharmacist-built guide to Levonorgestrel: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • It comes in two main types. The intrauterine systems (Mirena, Liletta, Kyleena, Skyla) prevent pregnancy for years, and Mirena and Liletta also treat heavy menstrual bleeding. The...
  • Take it as soon as you can, within 72 hours (3 days) of unprotected sex. The sooner you take it, the better it works. If you vomit within 2 hours, call a healthcare professional to...
  • How do I take the emergency contraceptive tablet?
  • No. It's a backup method and isn't as effective as regular birth control. It also won't work if you're already pregnant, and it doesn't protect against HIV or other STDs.
📖 Read our full Levonorgestrel guide →

🕸️ Concept Web — How Levonorgestrel 1.5 MG Oral Tablet [PostDay One-S... Connects

One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept Levonorgestrel 1.5 MG Oral Tablet [PostDay One-Step] RxCUI 2049247

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 1

    The active substance itself — no strength, form, or brand attached yet.

    • Levonorgestrel 6373
  2. Brand names 1

    The same medicine's trade names. A brand name alone says nothing about strength or form.

    • PostDay One-Step 2049242
  3. Dose forms 9

    The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.

    • Levonorgestrel Oral Tablet 372591
    • Levonorgestrel Oral Product 1163477
    • Levonorgestrel Pill 1163478
    • Levonorgestrel Oral Tablet [PostDay One-Step] 2049244
    • PostDay One-Step Oral Product 2049245
    • PostDay One-Step Pill 2049246
    • Oral Tablet 317541
    • Oral Product 1151131
    • +1 more in this family
  4. Clinical & branded drugs 3

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

Showing up to 8 concepts per family — 13 of 14 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.

🔀 Generic ⇄ Brand Crosswalk

The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.

Generic (Clinical) Concepts

  • Levonorgestrel 1.5 MG Oral Tablet SCD · 483325
  • Levonorgestrel 1.5 MG SCDC · 483324
  • Levonorgestrel Oral Tablet SCDF · 372591
  • Levonorgestrel Oral Product SCDG · 1163477
  • Levonorgestrel Pill SCDG · 1163478

Brand-Name Concepts

  • Levonorgestrel 1.5 MG [PostDay One-Step] SBDC · 2049243
  • Levonorgestrel Oral Tablet [PostDay One-Step] SBDF · 2049244
  • PostDay One-Step Oral Product SBDG · 2049245
  • PostDay One-Step Pill SBDG · 2049246
  • PostDay One-Step BN · 2049242

📦 FDA Products & Package NDCs

4 products · 4 package NDCs
4 package NDCs map to RxCUI 2049247 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
Package NDC Package Brand / generic name Labeler Marketing start
69953-0617-42 1 BLISTER PACK in 1 CARTON (69953-617-42) / 1 mg in 1 BLIST... PostDay One-Step Rapha Pharmaceuticals, Inc. 2023-01-16
69953-0618-43 1 BLISTER PACK in 1 CARTON (69953-618-43) / 1 mg in 1 BLIST... PostDay One-Step Rapha Pharmaceuticals, Inc. 2023-11-21
69953-0628-60 1 BLISTER PACK in 1 CARTON (69953-628-60) / 1 mg in 1 BLIST... PostDay One-Step Rapha Pharmaceuticals, Inc. 2023-01-16
85506-0100-10 1 BLISTER PACK in 1 CARTON (85506-100-10) / 1 TABLET in 1 B... PostDay One-Step Home Health Brands, LLC 2025-04-28
Observed labelers: Rapha Pharmaceuticals, Inc. (3) · Home Health Brands, LLC (1) — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

🗃️ Sources & Limits

Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
  • A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
  • Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
  • Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
  • Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.