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Lisinopril and Hydrochlorothiazide 20 mg; 12.5 mg Tablet, 100-count — NDC 65862-044-00 (Billing 65862-0044-00)

by Aurobindo Pharma Limited · 100 TABLET in 1 BOTTLE

This is a package of 100 tablets of Lisinopril and Hydrochlorothiazide 20 mg; 12.5 mg Tablet from Aurobindo Pharma Limited, marketed since Mar 2006 and currently FDA-listed. It is the main listing for this product, which comes in 6 package sizes.

NDC 65862-0044-00
🏷️ FDA NDC (as labeled) 65862-044-00 billing pads the product segment with a zero
This package
Contains100-count Pack sizes6 compare ↓
Also priced by: Part D plans $0.1025/unit — full pricing hub ↓
Main listing for product 65862-044 · Also comes in: 30 tablets 65862-044-30 100 tablets 65862-044-01 500 tablets 65862-044-05 1000 tablets 65862-044-99 5000 tablets 65862-044-59
On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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

⚠️
Other active recalls for Lisinopril And Hydrochlorothiazide (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Jun 20, 2025 — Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg. (Lupin Pharmaceuticals Inc.) · FDA recall D-0532-2025
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 65862-044-00
Product NDC 65862-044
11-digit billing NDC 65862004400
SPL Set ID 94dc7ffc-e19c-4a17-89ed-e14efc071f78
DEA schedule Non-controlled
Marketing category DRUG FOR FURTHER PROCESSING
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2006-03-14
Dosage form TABLET
Substance LISINOPRIL; HYDROCHLOROTHIAZIDE

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GCN Seq No 000388
GCN 88000
HICL code 000131
Ingredient (HICL) Lisinopril/Hydrochlorothiazide
HIC1 code A
Therapeutic class — broad (HIC1) Cardiovascular System
HIC2 code A4
Therapeutic class — intermediate (HIC2) Antihypertensives
HIC3 code A4J
Therapeutic class — specific (HIC3) Ace Inhibitor-Thiazide Or Thiazide-Like Diuretic
AHFS code 24:32.04.00
AHFS class Angiotensin-Converting Enzyme Inhibitors
FDB label name LISINOPRIL-HCTZ 20-12.5 MG TAB
FDB brand name Lisinopril-Hydrochlorothiazide
Legend status F — Federal legend — prescription drug or device
Quick answers
  • GSN (GCN sequence number): 000388
  • GCN: 88000
  • HICL (First Databank): 000131
  • AHFS class code: 24:32.04.00
Why two NDCs? The FDA registers this code as 65862-044-00 — a 5-3-2 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 product segment → 65862-0044-00. 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.

Clinical

Label name LISINOPRIL-HCTZ 20-12.5 MG TAB Ingredient Lisinopril/Hydrochlorothiazide
📗 Our plain-language guide HelloPharmacist
  • Great question. Lisinopril relaxes your blood vessels by blocking a chemical that causes them to tighten. Hydrochlorothiazide helps your kidneys remove extra salt and fluid. Togeth...
  • What exactly is this medication doing for me — why do I need two drugs in one pill?
  • Yes, that cough is a known side effect of the lisinopril part of this combination. It's not dangerous, but it can be really annoying. Don't just stop the medication on your own — t...
  • I've noticed a dry, nagging cough since I started this. Is that from the medication?
📖 Read our full Lisinopril and Hydrochlorothiazide guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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 $0.1025 $10.25 / 100 tablets
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
65862-0044-00 You're viewing this Main listing 100 TABLET in 1 BOTTLE 2006-03-14 — Active
65862-0044-01 65862-044-01 100 TABLET in 1 BOTTLE 2006-03-14 — Active
65862-0044-05 65862-044-05 500 TABLET in 1 BOTTLE 2006-03-14 — Active
65862-0044-30 65862-044-30 30 TABLET in 1 BOTTLE 2006-03-14 — Active
65862-0044-99 65862-044-99 1000 TABLET in 1 BOTTLE 2006-03-14 — Active
65862-0044-59 65862-044-59 5000 TABLET in 1 BAG — — Active

Pack size FAQ

What quantity is in this package?
This is a 100-count package — 100 tablet in 1 bottle.
How does this package differ from NDC 65862-0044-30?
Both are Lisinopril and Hydrochlorothiazide 20 mg; 12.5 mg Tablet — the drug itself is identical. This page's package is the 100-count one, while NDC 65862-0044-30 is the 30 tablets package.
What NDC number is used to bill for this package of Lisinopril and Hydrochlorothiazide 20 mg; 12.5 mg Tablet?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Lisinopril and hydrochlorothiazide 20 mg/1; 12.5 mg 00591-0861-01 Actavis 100 tablets $0.036 — Availability likely —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 43547-0421-10 Solco 100 tablets $0.036 AB Availability likely —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 68180-0519-01 Lupin 100 tablets $0.036 AB Availability likely —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 68645-0557-54 Legacy 30 tablets $0.036 AB Availability likely —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 76282-0447-01 Exelan 100 tablets $0.036 AB Availability likely —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 43063-0458-30 PD-Rx 30 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 50090-6204-00 A-S 30 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 50090-6752-00 A-S 90 tablets — AB FDA listed —
LISINOPRIL and HYDROCHLOROTHIAZIDE 20 mg/1; 12.5 mg 51407-0565-05 GSMS, 500 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 51655-0311-26 Northwind 90 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 51655-0414-26 Northwind 90 tablets — AB FDA listed —
Zestoretic 20 mg/1; 12.5 mg 52427-0436-90 Almatica 90 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 60760-0519-90 St. 90 tablets — AB FDA listed —
Lisinopril and hydrochlorothiazide 20 mg/1; 12.5 mg 63187-0050-00 Proficient 100 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 63629-4470-01 Bryant 30 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mgthis 65862-0044-00 Aurobindo 100 tablets — — FDA listed —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 67046-0433-03 Coupler 30 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 68071-2263-09 NuCare 90 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 68071-3177-03 NuCare 30 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 68071-4435-03 NuCare 30 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 68788-8253-01 Preferred 100 tablets — AB FDA listed —
Lisinopril And Hydrochlorothiazide 12.5 mg/1; 20 mg 68788-9809-01 Preferred 100 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 69097-0969-05 Cipla 90 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 70518-0382-00 REMEDYREPACK 90 tablets — AB Discontinued —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 70518-3505-00 REMEDYREPACK 90 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 71205-0022-00 Proficient 100 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 71205-0763-30 Proficient 30 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 71335-0862-01 Bryant 30 tablets — AB Discontinued —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 71335-9730-01 Bryant 30 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 71610-0274-80 Aphena 180 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 71610-0374-60 Aphena 90 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 12.5 mg/1; 20 mg 71610-0838-30 Aphena 30 tablets — AB FDA listed —
Lisinopril and Hydrochlorothiazide 20 mg/1; 12.5 mg 71610-0868-60 Aphena 90 tablets — AB FDA listed —
Lisinopril/HCTZ 20 mg/1; 12.5 mg 72189-0651-30 Direct_Rx 30 tablets — AB FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
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

🏛️
2006
On the market since
Mar 2006
📍
2026
Currently FDA-listed
20 years listed
🔓
·
Generic versions listed
see equivalents
✅Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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.

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

LabelerAurobindo Pharma Limited
Labeler code65862
First marketedMar 2006
Product typeDrug For Further Processing
Portfolio1,456 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 FDA label FDA SPL

The complete FDA label for this product, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label
📄 FDA label 19 words ▾

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

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

About this NDC listing & data coverage

Listed for further processing / repackaging

What "drug for further processing" means

FDA lists this package under the "drug for further processing" marketing category: Aurobindo Pharma Limited supplies it to other companies for further processing or repackaging (blister cards that are later repackaged or co-packaged are a common example). The units themselves are a finished dosage form — which is why pricing or Medicaid data can still appear — but this exact package code may not be the presentation a retail pharmacy dispenses.

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 — Not published for this NDC No photo available yet for this listing.
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

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Drug For Further Processing". Products approved under an application carry an NDA, ANDA, or BLA number.
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 Aurobindo Pharma Limited. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 5 other package presentations of this same product, including 30 tablets (65862-0044-30), 100 tablets (65862-0044-01), 500 tablets (65862-0044-05). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Aurobindo Pharma 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.
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.
← 65862-0043-00 · Aurobindo 65862-0045-00 · Aurobindo →
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.