24 HR tramadol hydrochloride 200 MG Extended Release Oral Tablet — RxCUI 833711
RxNorm drug concept · Semantic clinical drug
RxCUI 833711
Semantic clinical drug · SCD
● Current RxNorm concept 29 FDA products
69 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
RxCUI833711
Official name24 HR tramadol hydrochloride 200 MG Extended Release Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known astramadol HCl 200 MG 24 HR Extended Release Oral Tablet; traMADol HCl 200 MG 24HR Extended Release Oral Tablet
FDA products mapped29
Package NDCs mapped69
Reported Medicaid activity (SDUD)25,917 prescriptions · 44 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 Tramadol: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Yes — tramadol is a real opioid, though it works a little differently from something like morphine or oxycodone. It's prescribed for adults with pain that's severe enough that regu...
- What is tramadol actually used for? Is it a real opioid?
- Swallow it whole, once a day, at roughly the same time every day. This part is really important: never chew, crush, split, or dissolve the tablet — the extended-release design slow...
- How do I take the extended-release tablet correctly?
🕸️ Concept Web — How 24 HR tramadol hydrochloride 200 MG Extended Rel... 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
24 HR tramadol hydrochloride 200 MG Extended Release Oral Tablet
RxCUI 833711 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.
-
Tramadol
10689IN -
Tramadol hydrochloride
82110PIN
-
Tramadol
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Ultram
220606BN
-
Ultram
-
Dose forms 13
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Tramadol Extended Release Oral Tablet
374174SCDF -
Tramadol hydrochloride Extended Release Oral Tablet
2645951SCDFP -
Tramadol Oral Product
1157662SCDG -
Tramadol Pill
1157663SCDG -
Tramadol hydrochloride Oral Product
2661517SCDGP -
Tramadol hydrochloride Pill
2659527SCDGP -
Tramadol Extended Release Oral Tablet [Ultram]
616518SBDF -
Tramadol hydrochloride Extended Release Oral Tablet [Ultram]
2656690SBDFP - +5 more in this family
-
Tramadol Extended Release Oral Tablet
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Tramadol hydrochloride 200 MG
831437SCDC -
24 HR tramadol hydrochloride 200 MG Extended Release Oral Tablet [Ultram]
845315SBD -
Tramadol hydrochloride 200 MG [Ultram]
836402SBDC
-
Tramadol hydrochloride 200 MG
Showing up to 8 concepts per family — 14 of 19 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
-
Tramadol hydrochloride 200 MG
SCDC · 831437 -
Tramadol Extended Release Oral Tablet
SCDF · 374174 -
Tramadol hydrochloride Extended Release Oral Tablet
SCDFP · 2645951 -
Tramadol Oral Product
SCDG · 1157662 -
Tramadol Pill
SCDG · 1157663 -
Tramadol hydrochloride Oral Product
SCDGP · 2661517 -
Tramadol hydrochloride Pill
SCDGP · 2659527
Brand-Name Concepts
-
24 HR tramadol hydrochloride 200 MG Extended Release Oral Tablet [Ultram]
SBD · 845315 -
Tramadol hydrochloride 200 MG [Ultram]
SBDC · 836402 -
Tramadol Extended Release Oral Tablet [Ultram]
SBDF · 616518 -
Tramadol hydrochloride Extended Release Oral Tablet [Ultram]
SBDFP · 2656690 -
Ultram Oral Product
SBDG · 1187716 -
Ultram Pill
SBDG · 1187717 -
Ultram
BN · 220606
📦 FDA Products & Package NDCs
29 products · 69 package NDCs
69 package NDCs map to RxCUI 833711 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 |
|---|---|---|---|---|
| 76420-0244-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-30) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2022-07-25 |
| 76420-0244-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-60) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2022-07-25 |
| 76420-0244-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-90) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2022-07-25 |
| 76420-0245-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-245-30) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2022-07-25 |
| 76420-0245-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-245-60) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2022-07-25 |
| 76420-0245-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-245-90) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2022-07-25 |
| 76420-0246-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-246-30) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2022-07-25 |
| 76420-0536-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-30) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2023-02-16 |
| 76420-0536-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-60) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2023-02-16 |
| 76420-0536-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-90) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2023-02-16 |
| 76420-0537-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-537-30) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2023-02-16 |
| 76420-0537-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-537-60) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2023-02-16 |
| 76420-0537-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-537-90) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2023-02-16 |
| 76420-0538-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-538-30) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2023-02-16 |
| 76420-0538-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-538-60) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2023-02-16 |
| 76420-0538-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-538-90) | TRAMADOL HYDROCHLORIDE | Asclemed USA, Inc. | 2023-02-16 |
| 80425-0136-01 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0136-1) | Tramadol HCL ER | Advanced Rx Pharmacy of Tennessee, LLC | 2023-05-22 |
| 80425-0136-02 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0136-2) | Tramadol HCL ER | Advanced Rx Pharmacy of Tennessee, LLC | 2014-08-19 |
| 83008-0009-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (83008-009-30) | TRAMADOL HYDROCHLORIDE | Quality Care Products, LLC | 2023-03-03 |
Observed labelers:
Asclemed USA, Inc. (16) ·
Sun Pharmaceutical Industries, Inc. (12) ·
Macleods Pharmaceuticals Limited (9) ·
Bryant Ranch Prepack (8) ·
DIRECT RX (7) ·
Proficient Rx LP (6)
· +5 more — 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.