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Amlodipine Besylate and Benazepril Hydrochloride 5 mg; 10 mg Capsule, 90-count

by REMEDYREPACK INC. · 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4499-0)
NDC 70518-4499-00
🏷️ FDA NDC (as labeled) 70518-4499-0 billing pads the package segment with a zero
Rx only Generic On market Non-controlled
🗂️ Data synced Sep 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

FDA NDC (as labeled) 70518-4499-0
Product NDC 70518-4499
11-digit billing NDC 70518449900
Application # ANDA077183
SPL Set ID 5b750966-7b16-6d13-e063-6394a90a5800
Established class (EPC) Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Ch
Mechanism of action Angiotensin-converting Enzyme Inhibitors; Calcium Channel Antagonists; Cytochrome P450 3A Inhibitors
Physiologic effect Decreased Blood Pressure
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-10-11
Route ORAL
Dosage form CAPSULE
Substance AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
GCN Seq No 023769
GCN 33092
HICL code 010041
Ingredient (HICL) Amlodipine Besylate/Benazepril
HIC1 code A
Therapeutic class — broad (HIC1) Cardiovascular System
HIC2 code A4
Therapeutic class — intermediate (HIC2) Antihypertensives
HIC3 code A4K
Therapeutic class — specific (HIC3) Ace Inhibitor-Calcium Channel Blocker Combination
AHFS code 24:08.92.00
AHFS class Vasodilating Agents, Misc (24:08)
FDB label name AMLODIPINE-BENAZEPRIL 5-10 MG
FDB brand name Amlodipine Besylate-Benazepril
Legend status F — Federal legend — prescription drug or device
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 70518-4499-0 — 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 → 70518-4499-00. 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.

🏭 Manufacturer & labeler

LabelerREMEDYREPACK INC.
Application holderDR REDDYS LABORATORIES INC
FDA applicationANDA077183 (ANDA)
Labeler code70518
First marketedOct 2025
Product typeHuman Prescription Drug
Portfolio1,520 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.

🩺 Clinical

Label name AMLODIPINE-BENAZEPRIL 5-10 MG Ingredient Amlodipine Besylate/Benazepril
📖 What it is MedlinePlus · NLM

The combination of amlodipine and benazepril is used to treat high blood pressure. Amlodipine is in a class of medications called calcium channel blockers. It works by relaxing the blood vessels so the heart does not have to pump as hard. Benazepril is in a class of medications called angiotensin-converting enzyme (ACE) inhibitors. It works by decreasing certain chemicals that tighten the blood vessels, so blood flows more smoothly. High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys and other parts of the body. Damage to...

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • Yes, it's very common. Many people need more than one medicine to get their blood pressure under good control. Amlodipine and benazepril work through two completely different pathw...
  • Why am I taking two blood pressure medicines in one pill? Is that normal?
  • Yes, a dry persistent cough is a well-known side effect of ACE inhibitors like benazepril, the second ingredient in this combination. It's not dangerous, but it can be annoying. Do...
  • I've developed a dry, nagging cough since starting this medicine. Is that normal?
📖 Read our full Amlodipine and Benazepril 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.

🧪 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.

💲 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 $0.2794 $25.15 / 90 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Amlodipine and Benazepril Hydrochloride 5 mg/1; 10 mg 23155-0921-01 Heritage 100 capsules $0.102 AB Availability likely —
Amlodipine Besylate and Benazepril Hydrochloride 5 mg/1; 10 mg 55111-0339-01 Dr.Reddy's 100 capsules $0.102 AB Availability likely —
Amlodipine and Benazepril Hydrochloride 5 mg/1; 10 mg 57237-0143-01 Rising 100 capsules $0.102 AB Availability likely —
Amlodipine and Benazepril Hydrochloride 5 mg/1; 10 mg 65862-0583-01 Aurobindo 100 capsules $0.102 AB Availability likely —
Amlodipine Besylate and Benazepril Hydrochloride 5 mg/1; 10 mg 68001-0133-00 BluePoint 100 capsules $0.102 AB Availability likely —
Amlodipine Besylate and Benazepril Hydrochloride 5 mg/1; 10 mg 68180-0756-01 Lupin 100 capsules $0.102 AB Availability likely —
Lotrel 5 mg/1; 10 mg 00078-0405-05 Novartis 100 capsules $11.555 — Availability likely —
Amlodipine Besylate and Benazepril Hydrochloride 5 mg/1; 10 mg 50090-5404-00 A-S 30 capsules — AB FDA listed —
Amlodipine and Benazepril Hydrochloride 5 mg/1; 10 mg 50090-6770-00 A-S 30 capsules — AB FDA listed —
Amlodipine Besylate and Benazepril Hydrochloride 5 mg/1; 10 mg 69238-2685-01 Amneal 100 capsules — — FDA listed —
Amlodipine and Benazepril Hydrochloride 5 mg/1; 10 mg 70518-1928-00 REMEDYREPACK 90 capsules — AB FDA listed —
Amlodipine Besylate and Benazepril Hydrochloride 5 mg/1; 10 mgthis 70518-4499-00 REMEDYREPACK 90 capsules — AB FDA listed —
Amlodipine Besylate and Benazepril Hydrochloride 5 mg/1; 10 mg 71335-2634-01 Bryant 30 capsules — AB FDA listed —
Amlodipine Besylate and Benazepril Hydrochloride 5 mg/1; 10 mg 72789-0432-90 PD-Rx 90 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

🏛️
2025
On the market since
Oct 2025
📍
2026
Currently FDA-listed
1 year 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
70518-4499-00 You're viewing this 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4499-0) 2025-10-11 Active

🧭 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 — 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 ✓ Available
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 FDA registers it as 70518-4499-0, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 70518-4499-00, written without dashes as 70518449900. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 70518-4499-00, the first segment (70518) is the labeler code FDA assigned to REMEDYREPACK INC.; the middle segment (4499) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) identifies this exact package size and type. Together they name one specific package of one specific product.
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 REMEDYREPACK INC.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
REMEDYREPACK INC. 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.

📄 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.
📄 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 ↗
← 70518-4498-00 · REMEDYREPACK 70518-4500-00 · REMEDYREPACK →
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.