Home › NDC Lookup › Ingredients › Doxycycline › 70518-4762-00
💊image loading
(from DailyMed)

Doxycycline 100 mg Capsule, 14-count — NDC 70518-4762-0 (Billing 70518-4762-00) · Product 70518-4762

by REMEDYREPACK INC. · 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-4762-0)

NDC 70518-4762-0 (billing 70518-4762-00) is a package of 14 capsules of Doxycycline 100 mg Capsule from REMEDYREPACK INC., marketed since Sep 2026 and currently FDA-listed. It is the main listing for product NDC 70518-4762, its only package size.

NDC 70518-4762-00
🏷️ FDA NDC (as labeled) 70518-4762-0 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 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70518-4762-0
Product NDC 70518-4762
11-digit billing NDC 70518476200
Application # ANDA065055
SPL Set ID 5c27b19f-24d6-bef4-e063-6394a90a071f
Established class (EPC) Tetracycline-class Drug
Chemical class Tetracyclines
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-09-23
Route ORAL
Dosage form CAPSULE
Substance DOXYCYCLINE
TE code (Orange Book) AB · RLD · RS
Quick answers for NDC 70518-4762-0
  • 11-digit billing NDC: 70518476200
Why two NDCs? The FDA registers this code as 70518-4762-0 — 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 → 70518-4762-00. 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

📗 Our plain-language guide HelloPharmacist
  • It is an antibiotic for bacterial infections such as rickettsial infections, sexually transmitted infections, respiratory tract infections and eye infections. Some products are als...
  • Take it exactly as your prescriber and label say. Swallow capsules with a full glass of water and avoid taking them right before lying down. For one capsule product, take it at lea...
  • Diarrhea, nausea, vomiting, stomach upset and loss of appetite are the most common. You may also sunburn much more easily, so cover up and avoid tanning beds. Call me or your docto...
  • Call right away for severe or watery diarrhea, a blistering or peeling rash, headache with vision changes, trouble swallowing, or signs of an allergic reaction. Diarrhea can show u...
📖 Read our full Doxycycline guide →
7
Nutrient depletion considerations

Doxycycline may be associated with lower levels of 7 nutrients — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Doxycycline nutrient depletion report →
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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 · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
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
70518-4762-00 70518-4762-0 You're viewing this Main listing 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-4762-0) 2026-09-23 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Doxycycline 100 mg 60687-0716-21 American 30 capsules $0.227 AB Availability likely —
Doxycycline 100 mg 60687-0943-21 American 30 capsules $0.227 AB Availability likely —
Doxycycline 100 mg 64380-0922-01 Strides 50 capsules $0.227 AB Availability likely —
doxycycline 100 mg 50268-0281-15 AvPAK 50 capsules $0.227 AB Availability likely —
Doxycycline 100 mg 64380-0180-01 Strides 50 capsules $0.227 AB Availability likely —
Doxycycline 100 mg 68180-0652-08 Lupin 50 capsules $0.227 AB Availability likely —
doxycycline 100 mg 63187-0712-14 Proficient 14 capsules — AB FDA listed —
Doxycycline 100 mg 46708-0250-30 Alembic 30 capsules — AB FDA listed —
Doxycycline 100 mg 50090-6783-00 A-S 20 capsules — AB FDA listed —
Doxycycline 100 mg 68071-3752-02 NuCare 20 capsules — AB FDA listed —
Doxycycline 100 mg 71335-2417-00 Bryant 2 capsules — AB FDA listed —
Doxycycline 100 mg 71335-3064-00 Bryant 2 capsules — AB FDA listed —
Doxycycline 100 mg 61919-0276-20 DIRECT 20 capsules — — FDA listed —
doxycycline 100 mg 65841-0823-01 Zydus 100 capsules — AB FDA listed —
Doxycycline 100 mg 71335-1988-00 Bryant 2 capsules — AB FDA listed —
Doxycycline 100 mg 82804-0171-06 Proficient 6 capsules — AB FDA listed —
Doxycycline 100 mg 62332-0250-30 Alembic 30 capsules — AB FDA listed —
Doxycycline 100 mg 70518-0213-00 REMEDYREPACK 30 capsules — AB FDA listed —
Doxycycline 100 mg 43386-0792-02 Lupin 250 capsules — — FDA listed —
Doxycycline 100 mg 82804-0050-02 Proficient 2 capsules — AB FDA listed —
doxycycline 100 mg 50090-4833-00 A-S 20 capsules — AB FDA listed —
doxycycline 100 mg 68382-0707-01 Zydus 100 capsules — AB FDA listed —
Doxycycline 100 mg 51655-0711-20 Northwind 20 capsules — AB FDA listed —
Doxycycline 100 mg 68071-2152-02 NuCare 20 capsules — AB FDA listed —
doxycycline 100 mg 72789-0491-14 PD-Rx 14 capsules — AB FDA listed —
Doxycycline 100 mg 63187-0672-02 Proficient 2 capsules — AB FDA listed —
Doxycycline 100 mg 63304-0616-01 Sun 100 capsules — AB FDA listed —
doxycycline 100 mg 72789-0496-02 PD-Rx 2 capsules — AB FDA listed —
doxycycline 100 mg 67046-1260-03 Coupler 30 capsules — AB FDA listed —
doxycycline 100 mg 48433-0159-03 Safecor 30 capsules — AB FDA listed —
Doxycycline 100 mgthis 70518-4762-00 REMEDYREPACK 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

🏛️
2026
On the market since
Sep 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
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.

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

LabelerREMEDYREPACK INC.
Application holderSTRIDES PHARMA INTERNATIONAL AG
FDA applicationANDA065055 (ANDA)
Labeler code70518
First marketedSep 2026
Product typeHuman Prescription Drug
Portfolio1,527 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.
📄 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

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 70518-4762-0, 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: 70518-4762-00, written without dashes as 70518476200. 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 70518-4762-00, the first segment (70518) is the labeler code FDA assigned to REMEDYREPACK INC.; the middle segment (4762) 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.
← 70518-4761-00 · REMEDYREPACK 70518-4763-00 · 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.