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dimethyl fumarate 120 mg Capsule, Delayed Release, 14-count — NDC 70771-1530-07 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

dimethyl fumarate 120 mg Capsule, Delayed Release, 14-count — NDC 70771-1530-7 (Billing 70771-1530-07)

by Zydus Lifesciences Limited · 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

This is a package of 14 capsules of dimethyl fumarate 120 mg Capsule, Delayed Release from Zydus Lifesciences Limited, marketed since Sep 2020 and currently FDA-listed. It is this product's only package size.

NDC 70771-1530-07
🏷️ FDA NDC (as labeled) 70771-1530-7 billing pads the package segment with a zero
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70771-1530-7
Product NDC 70771-1530
11-digit billing NDC 70771153007
RxCUI 1373483, 1373491, 1373497
UNII FO2303MNI2
Application # ANDA210538
SPL Set ID 7203a262-de0f-42dd-b4fb-8856758b82e9
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-09-28
Route ORAL
Dosage form CAPSULE, DELAYED RELEASE
Substance DIMETHYL FUMARATE
Quick answers
  • RxCUI (RxNorm): 1373483
Why two NDCs? The FDA registers this code as 70771-1530-7 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 70771-1530-07. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Other immunosuppressants class.

Drug family (ATC) Other immunosuppressants
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📗 Our plain-language guide HelloPharmacist
  • The oral capsules are for relapsing forms of multiple sclerosis in adults. That includes clinically isolated syndrome, relapsing-remitting disease and active secondary progressive...
  • You take them by mouth twice a day. Most people start on a lower dose for the first week and then move up. Swallow them whole, and do not crush, chew or sprinkle them on food. Take...
  • Flushing is the most common, along with stomach pain, diarrhea and nausea. Taking the capsules with food can help the flushing. Your doctor may also suggest a non-enteric coated as...
  • Get emergency help for swelling of the face, lips or throat or trouble breathing, and do not take another dose. Call right away for new neurologic symptoms, signs of a serious infe...
📖 Read our full Dimethyl Fumarate guide →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · Q2 2026 $1.89 $26.39 / 14 capsules
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
70771-1530-07 You're viewing this Main listing 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE Sample 2020-09-28 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Dimethyl Fumarate 120 mg 31722-0657-31 Camber 14 capsules $0.428 AB Availability likely —
Dimethyl Fumarate 120 mg 43547-0024-14 Solco 14 capsules $0.428 AB Availability likely —
Dimethyl Fumarate 120 mg 43598-0429-52 Dr. 14 capsules $0.428 AB Availability likely —
Dimethyl Fumarate 120 mg 59651-0083-14 Aurobindo 14 capsules $0.428 AB Availability likely —
Dimethyl Fumarate 120 mg 69097-0322-89 Cipla 14 capsules $0.428 — Availability likely —
Dimethyl Fumarate 120 mg 69238-1318-04 Amneal 14 capsules $0.428 AB Availability likely —
Dimethyl Fumarate 120 mg 70512-0852-14 SOLA 14 capsules $0.428 AB Availability likely —
Dimethyl fumarate 120 mg 82249-0745-14 CivicaScript 14 capsules $0.428 AB Availability likely —
Dimethyl Fumarate 120 mg 16729-0416-04 Accord 14 capsules $0.617 AB Availability likely —
dimethyl fumarate 120 mg 24979-0127-02 Upsher-Smith 500 capsules — AB FDA listed —
Dimethyl Fumarate 120 mg 33342-0349-09 Macleods 60 capsules — AB FDA listed —
dimethyl fumarate 120 mg 51407-0442-14 Golden 14 capsules — AB FDA listed —
Tecfidera 120 mg 64406-0005-01 Biogen 14 capsules — AB FDA listed —
Dimethyl fumarate 120 mg 67877-0555-10 Ascend 1000 capsules — AB FDA listed —
Dimethyl Fumarate 120 mg 68462-0307-05 Glenmark 500 capsules — AB FDA listed —
Dimethyl Fumarate 120 mg 69539-0042-05 MSN 500 capsules — AB FDA listed —
dimethyl fumarate 120 mg 70710-1204-07 Zydus 14 capsules — — FDA listed —
dimethyl fumarate 120 mgthis 70771-1530-07 Zydus 14 capsules — — FDA listed —
Dimethyl Fumarate 120 mg 84677-0029-14 Golden 14 capsules — AB FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2020
On the market since
Sep 2020
📍
2026
Currently FDA-listed
6 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color Green / White
ShapeCapsule
Imprint1205
Size22 mm
ScoringNot scored
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerZydus Lifesciences Limited
Application holderZYDUS PHARMACEUTICALS USA INC
FDA applicationANDA210538 (ANDA)
Labeler code70771
First marketedSep 2020
Product typeHuman Prescription Drug
Portfolio720 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 Package Label / Principal Display Panel
📄 Package Label / Principal Display Panel 56 words ▾

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1532-3 30-Day Starter Pack Carton Label Dimethyl Fumarate Delayed-release Capsules 120 mg Starter Dose: 14 Capsules 240 mg Regular Dose: 46 Capsules Rx only NDC 70771-1530-7 Dimethyl Fumarate Delayed-release Capsules, 120 mg 14 Capsules Rx only NDC 70771-1531-6 Dimethyl Fumarate Delayed-release Capsules, 240 mg 60 Capsules Rx only label label label

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Dimethyl Fumarate — the program that covers self-administered drugs. 12 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Dimethyl Fumarate. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$10.94M
Claims incl. refills
14.9K
Beneficiaries
6.3K
Spend / beneficiary
$1,737.88
Spend / claim
$733.91
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

About this NDC listing & data coverage

Finished prescription product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Zydus Lifesciences Limited. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Zydus Lifesciences Limited is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 70771-1529-00 · Zydus 70771-1531-06 · Zydus →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.