24 HR tofacitinib 22 MG Extended Release Oral Tablet — RxCUI 2273113
RxNorm drug concept · Semantic clinical drug
RxCUI 2273113
Semantic clinical drug · SCD
● Current RxNorm concept 14 FDA products
18 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
RxCUI2273113
Official name24 HR tofacitinib 22 MG Extended Release Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known astofacitinib 22 MG 24HR Extended Release Oral Tablet
FDA products mapped14
Package NDCs mapped18
Reported Medicaid activity (SDUD)41,140 prescriptions · 51 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 Tofacitinib: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- It treats rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis and ulcerative colitis in adults, usually after a TNF blocker didn't work or wasn't tolerated. Xeljanz a...
- You take it by mouth. Tablets and solution are usually taken twice a day, and extended-release tablets once a day. It can be taken with or without food. Follow your prescriber's di...
- Colds, stuffy or sore nose and throat, diarrhea, and headache are most common. Some people with ulcerative colitis also get rash, shingles, or higher cholesterol. Call your doctor...
- Get help right away for chest pain, stroke symptoms, sudden shortness of breath, or leg swelling and pain, which can signal a clot or heart problem. Also report new belly pain, sig...
🕸️ Concept Web — How 24 HR tofacitinib 22 MG Extended Release Oral Ta... 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 tofacitinib 22 MG Extended Release Oral Tablet
RxCUI 2273113 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
-
Tofacitinib
1357536IN
-
Tofacitinib
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Xeljanz
1357542BN
-
Xeljanz
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Tofacitinib Extended Release Oral Tablet
1741045SCDF -
Tofacitinib Oral Product
1357538SCDG -
Tofacitinib Pill
1357539SCDG -
Tofacitinib Extended Release Oral Tablet [Xeljanz]
1741048SBDF -
Xeljanz Oral Product
1357545SBDG -
Xeljanz Pill
1357546SBDG -
Extended Release Oral Tablet
316945DF -
Oral Product
1151131DFG - +1 more in this family
-
Tofacitinib Extended Release Oral Tablet
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Tofacitinib 22 MG
2273112SCDC -
24 HR tofacitinib 22 MG Extended Release Oral Tablet [Xeljanz]
2273115SBD -
Tofacitinib 22 MG [Xeljanz]
2273114SBDC
-
Tofacitinib 22 MG
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
-
Tofacitinib 22 MG
SCDC · 2273112 -
Tofacitinib Extended Release Oral Tablet
SCDF · 1741045 -
Tofacitinib Oral Product
SCDG · 1357538 -
Tofacitinib Pill
SCDG · 1357539
Brand-Name Concepts
-
24 HR tofacitinib 22 MG Extended Release Oral Tablet [Xeljanz]
SBD · 2273115 -
Tofacitinib 22 MG [Xeljanz]
SBDC · 2273114 -
Tofacitinib Extended Release Oral Tablet [Xeljanz]
SBDF · 1741048 -
Xeljanz Oral Product
SBDG · 1357545 -
Xeljanz Pill
SBDG · 1357546 -
Xeljanz
BN · 1357542
📦 FDA Products & Package NDCs
14 products · 18 package NDCs
18 package NDCs map to RxCUI 2273113 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 |
|---|---|---|---|---|
| 00069-0501-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0... | XELJANZ XR | Pfizer Laboratories Div Pfizer Inc | 2016-03-07 |
| 00069-0502-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0... | XELJANZ XR | Pfizer Laboratories Div Pfizer Inc | 2020-01-21 |
| 00069-1001-01 | 60 TABLET, FILM COATED in 1 BOTTLE (0069-1001-01) | XELJANZ | Pfizer Laboratories Div Pfizer Inc | 2012-11-09 |
| 00069-1002-01 | 60 TABLET, FILM COATED in 1 BOTTLE (0069-1002-01) | XELJANZ | Pfizer Laboratories Div Pfizer Inc | 2018-07-02 |
| 00069-1029-02 | 1 BOTTLE in 1 CARTON (0069-1029-02) / 240 mL in 1 BOTTLE (0... | XELJANZ | Pfizer Laboratories Div Pfizer Inc | 2021-02-08 |
| 63539-0012-02 | 60 TABLET, FILM COATED in 1 BOTTLE (63539-012-02) | XELJANZ | U.S. Pharmaceuticals | 2012-11-08 |
| 63539-0016-02 | 60 TABLET, FILM COATED in 1 BOTTLE (63539-016-02) | XELJANZ | U.S. Pharmaceuticals | 2018-07-02 |
| 63539-0029-02 | 1 BOTTLE in 1 CARTON (63539-029-02) / 240 mL in 1 BOTTLE (6... | XELJANZ | U.S. Pharmaceuticals | 2021-02-08 |
| 63539-0501-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63539-501-30) | XELJANZ XR | U.S. Pharmaceuticals | 2016-03-07 |
| 63539-0502-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63539-502-30) | XELJANZ XR | U.S. Pharmaceuticals | 2020-01-21 |
| 70710-1353-03 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-... | tofacitinib | Zydus Pharmaceuticals USA Inc. | 2026-05-20 |
| 70710-1353-09 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-... | tofacitinib | Zydus Pharmaceuticals USA Inc. | 2026-05-20 |
| 70710-1727-03 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-... | tofacitinib | Zydus Pharmaceuticals USA Inc. | 2026-05-20 |
| 70710-1727-09 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-... | tofacitinib | Zydus Pharmaceuticals USA Inc. | 2026-05-20 |
| 70771-1627-03 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-... | tofacitinib | Zydus Lifesciences Limited | 2026-05-20 |
| 70771-1627-09 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-... | tofacitinib | Zydus Lifesciences Limited | 2026-05-20 |
| 70771-1628-03 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-... | tofacitinib | Zydus Lifesciences Limited | 2026-05-20 |
| 70771-1628-09 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-... | tofacitinib | Zydus Lifesciences Limited | 2026-05-20 |
Observed labelers:
Pfizer Laboratories Div Pfizer Inc (5) ·
U.S. Pharmaceuticals (5) ·
Zydus Lifesciences Limited (4) ·
Zydus Pharmaceuticals USA Inc. (4)
— 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.