Home › NDC Lookup › RxCUI directory › RxCUI 857706

Diclofenac sodium 50 MG / misoprostol 0.2 MG Delayed Release Oral Tablet — RxCUI 857706

RxNorm drug concept · Semantic clinical drug
RxCUI 857706 Semantic clinical drug · SCD ● Current RxNorm concept 19 FDA products 46 package NDCs Snapshot Jul 14, 2026

This page is curated, coded, and maintained by

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

RxCUI857706
Official nameDiclofenac sodium 50 MG / misoprostol 0.2 MG Delayed Release Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asdiclofenac sodium 50 MG / misoprostol 200 MCG Delayed Release Oral Tablet; diclofenac sodium (enteric coated core) 50 MG / misoprostol (non-enteric coated mantle) 200 MCG Oral Tablet
FDA products mapped19
Package NDCs mapped46
Reported Medicaid activity (SDUD)956 prescriptions · 7 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 Diclofenac Ophthalmic: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • Diclofenac sodium eye drops are an anti-inflammatory medication used after eye surgery. If you had cataract surgery, they help control swelling and inflammation in your eye during...
  • Yes, that's very common. About 15% of patients notice temporary burning or stinging right after applying the drop. It usually settles within a minute or so. If the burning is sever...
  • My eye burns a little when I put the drop in — is that normal?
  • While most side effects are mild, there have been rare but serious reports of corneal problems — including thinning or ulceration of the clear surface of the eye. If you notice sud...
📖 Read our full Diclofenac Ophthalmic guide →

🕸️ Concept Web — How Diclofenac sodium 50 MG / misoprostol 0.2 MG Del... 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 Diclofenac sodium 50 MG / misoprostol 0.2 MG Delayed Release Oral Tablet RxCUI 857706

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

  1. Ingredients 4

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

    • Diclofenac 3355
    • Misoprostol 42331
    • Diclofenac / misoprostol 214502
    • Diclofenac sodium 203214
  2. Brand names 1

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

    • Arthrotec 68373
  3. Dose forms 13

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

    • Diclofenac / misoprostol Delayed Release Oral Tablet 1808539
    • Diclofenac sodium / misoprostol Delayed Release Oral Tablet 2648311
    • Diclofenac / misoprostol Oral Product 1151144
    • Diclofenac / misoprostol Pill 1151145
    • Diclofenac sodium / misoprostol Oral Product 2660356
    • Diclofenac sodium / misoprostol Pill 2662431
    • Diclofenac / misoprostol Delayed Release Oral Tablet [Arthrotec] 1808541
    • Diclofenac sodium / misoprostol Delayed Release Oral Tablet [Arthrotec] 2654970
    • +5 more in this family
  4. Clinical & branded drugs 4

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

Showing up to 8 concepts per family — 17 of 22 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

  • Diclofenac sodium 50 MG SCDC · 855681
  • Misoprostol 0.2 MG SCDC · 316311
  • Diclofenac / misoprostol Delayed Release Oral Tablet SCDF · 1808539
  • Diclofenac sodium / misoprostol Delayed Release Oral Tablet SCDFP · 2648311
  • Diclofenac / misoprostol Oral Product SCDG · 1151144
  • Diclofenac / misoprostol Pill SCDG · 1151145
  • Diclofenac sodium / misoprostol Oral Product SCDGP · 2660356
  • Diclofenac sodium / misoprostol Pill SCDGP · 2662431

Brand-Name Concepts

  • Diclofenac sodium 50 MG / misoprostol 0.2 MG Delayed Release Oral Tablet [Arthrotec] SBD · 1359107
  • Diclofenac sodium 50 MG / misoprostol 0.2 MG [Arthrotec] SBDC · 855683
  • Diclofenac / misoprostol Delayed Release Oral Tablet [Arthrotec] SBDF · 1808541
  • Diclofenac sodium / misoprostol Delayed Release Oral Tablet [Arthrotec] SBDFP · 2654970
  • Arthrotec Oral Product SBDG · 1171432
  • Arthrotec Pill SBDG · 1171435
  • Arthrotec BN · 68373

📦 FDA Products & Package NDCs

19 products · 46 package NDCs
46 package NDCs map to RxCUI 857706 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
00025-1411-60 60 TABLET, FILM COATED in 1 BOTTLE (0025-1411-60) ARTHROTEC Pfizer Laboratories Div Pfizer Inc 1997-12-24
00025-1411-90 90 TABLET, FILM COATED in 1 BOTTLE (0025-1411-90) ARTHROTEC Pfizer Laboratories Div Pfizer Inc 1997-12-24
00025-1421-60 60 TABLET, FILM COATED in 1 BOTTLE (0025-1421-60) ARTHROTEC Pfizer Laboratories Div Pfizer Inc 1997-12-24
00591-0397-19 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0591-0397-1... Diclofenac Sodium and Misoprostol Actavis Pharma, Inc. 2012-11-01
00591-0397-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0591-0397-6... Diclofenac Sodium and Misoprostol Actavis Pharma, Inc. 2012-11-01
00591-0398-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0591-0398-6... Diclofenac Sodium and Misoprostol Actavis Pharma, Inc. 2012-11-01
42291-0232-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (42291-232-60) Diclofenac Sodium and Misoprostol AvKARE 2016-09-26
42291-0233-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (42291-233-60) Diclofenac Sodium and Misoprostol AvKARE 2012-12-14
42571-0133-29 60 BLISTER PACK in 1 CARTON (42571-133-29) / 10 TABLET in 1... Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL Micro Labs Limited 2021-09-01
42571-0133-30 30 TABLET in 1 BOTTLE (42571-133-30) Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL Micro Labs Limited 2021-09-01
42571-0133-60 60 TABLET in 1 BOTTLE (42571-133-60) Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL Micro Labs Limited 2021-09-01
42571-0133-90 90 TABLET in 1 BOTTLE (42571-133-90) Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL Micro Labs Limited 2021-09-01
42571-0134-29 60 BLISTER PACK in 1 CARTON (42571-134-29) / 10 TABLET in 1... Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL Micro Labs Limited 2021-09-01
42571-0134-30 30 TABLET in 1 BOTTLE (42571-134-30) Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL Micro Labs Limited 2021-09-01
42571-0134-60 60 TABLET in 1 BOTTLE (42571-134-60) Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL Micro Labs Limited 2021-09-01
42571-0134-90 90 TABLET in 1 BOTTLE (42571-134-90) Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL Micro Labs Limited 2021-09-01
59762-0028-01 60 TABLET, FILM COATED in 1 BOTTLE (59762-0028-1) Diclofenac sodium and Misoprostol Mylan Pharmaceuticals Inc. 2012-11-01
59762-0028-02 90 TABLET, FILM COATED in 1 BOTTLE (59762-0028-2) Diclofenac sodium and Misoprostol Mylan Pharmaceuticals Inc. 2012-11-01
59762-0029-01 60 TABLET, FILM COATED in 1 BOTTLE (59762-0029-1) Diclofenac sodium and Misoprostol Mylan Pharmaceuticals Inc. 2012-11-01
65162-0436-03 30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-436-03) Diclofenac Sodium and Misoprostol Amneal Pharmaceuticals LLC 2016-12-01
65162-0436-06 60 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-436-06) Diclofenac Sodium and Misoprostol Amneal Pharmaceuticals LLC 2016-12-01
65162-0436-09 90 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-436-09) Diclofenac Sodium and Misoprostol Amneal Pharmaceuticals LLC 2016-12-01
65162-0436-10 100 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-436-10) Diclofenac Sodium and Misoprostol Amneal Pharmaceuticals LLC 2016-12-01
65162-0438-03 30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-438-03) Diclofenac Sodium and Misoprostol Amneal Pharmaceuticals LLC 2016-12-01
65162-0438-06 60 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-438-06) Diclofenac Sodium and Misoprostol Amneal Pharmaceuticals LLC 2016-12-01
65162-0438-10 100 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-438-10) Diclofenac Sodium and Misoprostol Amneal Pharmaceuticals LLC 2016-12-01
68001-0231-06 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-231-0... Diclofenac Sodium and Misoprostol BluePoint Laboratories 2014-02-26
68001-0232-06 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-232-0... Diclofenac Sodium and Misoprostol BluePoint Laboratories 2014-02-26
71205-0865-00 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-00) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0865-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-30) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0865-55 500 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-55) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0865-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-60) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0865-64 240 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-64) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0865-72 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-72) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0865-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-90) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0866-00 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-00) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0866-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-30) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0866-55 500 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-55) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0866-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-60) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0866-64 240 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-64) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0866-72 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-72) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
71205-0866-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-90) Diclofenac Sodium Misoprostol Proficient Rx LP 2022-03-07
72162-2518-06 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2518-6) Diclofenac Sodium Misoprostol Bryant Ranch Prepack 2021-07-15
75834-0264-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (75834-264-60) Diclofenac Sodium Misoprostol Nivagen Pharmaceuticals, Inc. 2021-07-15
75834-0264-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (75834-264-90) Diclofenac Sodium Misoprostol Nivagen Pharmaceuticals, Inc. 2021-07-15
75834-0265-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (75834-265-60) Diclofenac Sodium Misoprostol Nivagen Pharmaceuticals, Inc. 2021-07-15
Observed labelers: Proficient Rx LP (14) · Micro Labs Limited (8) · Amneal Pharmaceuticals LLC (7) · Actavis Pharma, Inc. (3) · Mylan Pharmaceuticals Inc. (3) · Nivagen Pharmaceuticals, Inc. (3) · +4 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.

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.