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Hydroxyprogesterone caproate (USP) 250 MG/ML Injectable Solution — RxCUI 1087964

RxNorm drug concept · Semantic clinical drug
RxCUI 1087964 Semantic clinical drug · SCD ● Current RxNorm concept 1 FDA product 2 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

RxCUI1087964
Official nameHydroxyprogesterone caproate (USP) 250 MG/ML Injectable Solution
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asHYDROXYprogesterone caproate 250 MG/ML Injectable Solution
FDA products mapped1
Package NDCs mapped2
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

🕸️ Concept Web — How Hydroxyprogesterone caproate (USP) 250 MG/ML Inj... 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 Hydroxyprogesterone caproate (USP) 250 MG/ML Injectable Solution RxCUI 1087964

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

  1. Ingredients 2

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

    • 17-alpha-hydroxyprogesterone 5542
    • Hydroxyprogesterone caproate (USP) 12488
  2. Dose forms 6

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

    • 17-alpha-hydroxyprogesterone Injectable Solution 374662
    • Hydroxyprogesterone caproate (USP) Injectable Solution 2648784
    • 17-alpha-hydroxyprogesterone Injectable Product 1164632
    • Hydroxyprogesterone caproate (USP) Injectable Product 2660751
    • Injectable Solution 316949
    • Injectable Product 1151126
  3. Clinical & branded drugs 1

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

    • Hydroxyprogesterone caproate (USP) 250 MG/ML 1087963

Showing up to 8 concepts per family — 9 of 9 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

  • Hydroxyprogesterone caproate (USP) 250 MG/ML SCDC · 1087963
  • 17-alpha-hydroxyprogesterone Injectable Solution SCDF · 374662
  • Hydroxyprogesterone caproate (USP) Injectable Solution SCDFP · 2648784
  • 17-alpha-hydroxyprogesterone Injectable Product SCDG · 1164632
  • Hydroxyprogesterone caproate (USP) Injectable Product SCDGP · 2660751

📦 FDA Products & Package NDCs

1 product · 2 package NDCs
2 package NDCs map to RxCUI 1087964 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
55150-0311-01 1 VIAL in 1 CARTON (55150-311-01) / 5 mL in 1 VIAL Hydroxyprogesterone Caproate Eugia US LLC 2019-05-09
55150-0311-05 5 VIAL in 1 CARTON (55150-311-05) / 5 mL in 1 VIAL Hydroxyprogesterone Caproate Eugia US LLC 2019-05-09
Observed labelers: Eugia US LLC (2) — 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.