12 HR oxymorphone hydrochloride 40 MG Extended Release Oral Tablet — RxCUI 977915
RxNorm drug concept · Semantic clinical drug
RxCUI 977915
Semantic clinical drug · SCD
● Current RxNorm concept 14 FDA products
56 package NDCs
Snapshot Jul 14, 2026
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
RxCUI977915
Official name12 HR oxymorphone hydrochloride 40 MG Extended Release Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asoxyMORphone HCl 40 MG 12HR Extended Release Oral Tablet
FDA products mapped14
Package NDCs mapped56
Reported Medicaid activity (SDUD)2,486 prescriptions · 12 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Oxymorphone: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- The regular oxymorphone tablet is meant for short-term, acute pain — the kind that hits hard and needs quick relief for a limited time. You'd take it every four to six hours as nee...
- What's the difference between the regular tablet and the extended-release tablet?
- It's a real safety point, not just a suggestion. Eating a meal before taking oxymorphone — especially the extended-release version — can raise the amount of drug that gets into you...
- Why does my pharmacist keep telling me to take this on an empty stomach?
🕸️ Concept Web — How 12 HR oxymorphone hydrochloride 40 MG Extended R... 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
12 HR oxymorphone hydrochloride 40 MG Extended Release Oral Tablet
RxCUI 977915 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 2
The active substance itself — no strength, form, or brand attached yet.
-
Oxymorphone
7814IN -
Oxymorphone hydrochloride
82064PIN
-
Oxymorphone
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Oxymorphone Extended Release Oral Tablet
643115SCDF -
Oxymorphone hydrochloride Extended Release Oral Tablet
2645937SCDFP -
Oxymorphone Oral Product
1162252SCDG -
Oxymorphone Pill
1162253SCDG -
Oxymorphone hydrochloride Oral Product
2660073SCDGP -
Oxymorphone hydrochloride Pill
2659325SCDGP -
Extended Release Oral Tablet
316945DF -
Oral Product
1151131DFG - +1 more in this family
-
Oxymorphone Extended Release Oral Tablet
-
Clinical & branded drugs 1
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Oxymorphone hydrochloride 40 MG
977914SCDC
-
Oxymorphone hydrochloride 40 MG
Showing up to 8 concepts per family — 11 of 12 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
-
Oxymorphone hydrochloride 40 MG
SCDC · 977914 -
Oxymorphone Extended Release Oral Tablet
SCDF · 643115 -
Oxymorphone hydrochloride Extended Release Oral Tablet
SCDFP · 2645937 -
Oxymorphone Oral Product
SCDG · 1162252 -
Oxymorphone Pill
SCDG · 1162253 -
Oxymorphone hydrochloride Oral Product
SCDGP · 2660073 -
Oxymorphone hydrochloride Pill
SCDGP · 2659325
📦 FDA Products & Package NDCs
14 products · 56 package NDCs
56 package NDCs map to RxCUI 977915 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 |
|---|---|---|---|---|
| 64896-0700-08 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-... | Oxymorphone hydrochloride | Amneal Pharmaceuticals LLC | 2013-01-02 |
| 64896-0700-13 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-... | Oxymorphone hydrochloride | Amneal Pharmaceuticals LLC | 2013-01-02 |
| 64896-0701-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896... | Oxymorphone hydrochloride | Amneal Pharmaceuticals LLC | 2013-01-02 |
| 64896-0701-03 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (6489... | Oxymorphone hydrochloride | Amneal Pharmaceuticals LLC | 2013-01-02 |
| 64896-0701-08 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-... | Oxymorphone hydrochloride | Amneal Pharmaceuticals LLC | 2013-01-02 |
| 64896-0701-13 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-... | Oxymorphone hydrochloride | Amneal Pharmaceuticals LLC | 2013-01-02 |
Observed labelers:
Amneal Pharmaceuticals LLC (28) ·
Amneal Pharmaceuticals of New York LLC (28)
— 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.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.