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Chlordiazepoxide 25 mg Capsule, Gelatin Coated, 30-count — NDC 61919-593-30 (Billing 61919-0593-30)

by DIRECT RX · 30 CAPSULE, GELATIN COATED in 1 BOTTLE

This is a package of 30 capsules of Chlordiazepoxide 25 mg Capsule, Gelatin Coated from DIRECT RX, no longer marketed, no longer in the FDA NDC Directory. It is this product's only package size.

NDC 61919-0593-30
🏷️ FDA NDC (as labeled) 61919-593-30 billing pads the product segment with a zero
Rx only Generic Discontinued CIV ⚠ Inactivated by FDA ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 14, 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

NDC database record

One package, one record: these facts belong to NDC 61919-593-30 alone.

Record
FDA NDC Directory package listing · Human prescription drug
Code segments
61919 labeler · 593 product · 30 package
Billing quantity
30 EA per package
Barcode (UPC-A, from the NDC)
3 6191959330 5
FDA record last changed
Jul 14, 2026
⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2023. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 61919-593-30
Product NDC 61919-593
11-digit billing NDC 61919059330
NCPDP billing unit EA — each (per item)
Application # ANDA085475
SPL Set ID 2f1d49ad-13cb-2a23-e054-00144ff88e88
Chemical class Benzodiazepine [EPC], Benzodiazepines
DEA schedule CIV
Marketing category ANDA
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2023)
Route ORAL
Dosage form CAPSULE, GELATIN COATED
Substance CHLORDIAZEPOXIDE HYDROCHLORIDE
TE code (Orange Book) AB · RLD · RS

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

GCN Seq No 003735
GCN 14032
HICL code 001610
Ingredient (HICL) Chlordiazepoxide Hcl
HIC1 code H
Therapeutic class — broad (HIC1) Nervous System (Except Autonomic)
HIC2 code H2
Therapeutic class — intermediate (HIC2) Psychoactive Drugs
HIC3 code H20
Therapeutic class — specific (HIC3) Anti-Anxiety - Benzodiazepines
AHFS code 28:24.08.00
AHFS class Benzodiazepines (Anxiolytic,Sedativ/Hyp)
FDB label name CHLORDIAZEPOXIDE 25 MG CAPSULE
FDB brand name Chlordiazepoxide Hcl
Legend status F — Federal legend — prescription drug or device
Quick answers
  • GSN (GCN sequence number): 003735
  • GCN: 14032
  • HICL (First Databank): 001610
  • AHFS class code: 28:24.08.00
Why two NDCs? The FDA registers this code as 61919-593-30 — 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 → 61919-0593-30. 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 CHLORDIAZEPOXIDE 25 MG CAPSULE Ingredient Chlordiazepoxide Hcl
📗 Our plain-language guide HelloPharmacist
  • Chlordiazepoxide is mainly used for three things: managing anxiety disorders, easing the symptoms of going through alcohol withdrawal, and calming pre-surgery anxiety. It's not mea...
  • What exactly is chlordiazepoxide used for?
  • Please don't stop on your own — this is one of the most important things to know about this medicine. Your body can become physically dependent on chlordiazepoxide, and stopping su...
  • Can I stop taking it whenever I want if I feel better?
📖 Read our full Chlordiazepoxide 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 · 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
61919-0593-30 You're viewing this Main listing 30 CAPSULE, GELATIN COATED in 1 BOTTLE 2019-04-04 — Inactivated by FDA

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Chlordiazepoxide Hydrochloride 25 mg 00555-0159-02 Teva 100 capsules $0.158 AB Availability likely —
Chlordiazepoxide Hydrochloride 25 mg 51079-0141-20 Mylan 100 capsules $0.158 AB Availability likely —
Chlordiazepoxide Hydrochloride 25 mg 60687-0807-01 American 100 capsules $0.158 AB Availability likely —
Chlordiazepoxide Hydrochloride 25 mg 62135-0222-60 Chartwell 60 capsules $0.158 AB Availability likely —
Chlordiazepoxide Hydrochloride 25 mg 42806-0563-01 Epic 100 capsules $0.160 AB Availability likely —
Chlordiazepoxide Hydrochloride 25 mg 42806-0566-01 Epic 100 capsules $0.160 AB Availability likely —
Chlordiazepoxide Hydrochloride 25 mg 43063-0046-03 PD-Rx 3 capsules — AB FDA listed —
Chlordiazepoxide Hydrochloride 25 mg 48433-0020-20 Safecor 100 capsules — AB FDA listed —
Chlordiazepoxide Hydrochloride 25 mg 58118-1590-08 Clinical 30 capsules — AB FDA listed —
Chlordiazepoxide Hydrochloride 25 mg 67046-0910-03 Couper 30 capsules — AB FDA listed —
Chlordiazepoxide Hydrochloride 25 mg 68071-5171-03 NuCare 30 capsules — AB FDA listed —
Chlordiazepoxide Hydrochloride 25 mg 68071-5256-06 NuCare 6 capsules — AB FDA listed —
Chlordiazepoxide Hydrochloride 25 mg 70518-0015-00 REMEDYREPACK 30 capsules — AB FDA listed —
Chlordiazepoxide Hydrochloride 25 mg 70518-0157-01 REMEDYREPACK 100 capsules — AB Discontinued —
Chlordiazepoxide Hydrochloride 25 mg 87441-0015-01 Unit 30 capsules — AB FDA listed —
Chlordiazepoxide 25 mgthis 61919-0593-30 DIRECT 30 capsules — AB Discontinued —
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
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.

🧪 Avoiding an ingredient? See Chlordiazepoxide inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

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

LabelerDIRECT RX
Application holderBAUSCH HEALTH US LLC
FDA applicationANDA085475 (ANDA)
Labeler code61919
DEA scheduleCIV
Product typeHuman Prescription Drug
Portfolio204 products on file

More NDCs from DIRECT RX labeler code 61919

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. Very long sections are excerpted here and marked; the full text is on DailyMed (linked in the sources below). Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⛔ Contraindications ⚠️ Warnings 🤒 Adverse Reactions 🆘 Overdosage 🧬 Clinical Pharmacology 📦 Storage and Handling 📋 Description 💬 Medication Guide ⚠️ Precautions 🔒 Drug Abuse and Dependence 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 3 words ▾

INDICATIONS AND USAGE:

⏱️ Dosage and Administration 3 words ▾

DOSAGE AND ADMINISTRATION:

⛔ Contraindications 1 words ▾

CONTRAINDICATIONS:

⚠️ Warnings 1 words ▾

WARNINGS:

🤒 Adverse Reactions 2 words ▾

ADVERSE REACTIONS:

🆘 Overdosage 1 words ▾

OVERDOSAGE:

🧬 Clinical Pharmacology 2 words ▾

CLINICAL PHARMACOLOGY:

📦 Storage and Handling 3 words ▾

STORAGE AND HANDLING

📋 Description 1 words ▾

DESCRIPTION:

💬 Medication Guide ~3 min read ▾

Chlordiazepoxide Hydrochloride Capsules, USP C-IV What is the most important information I should know about chlordiazepoxide? • Chlordiazepoxide is a benzodiazepine medicine. Taking benzodiazepines with opioid medicines, alcohol, or other central nervous system depressants (including street drugs) can cause severe drowsiness, breathing problems (respiratory depression), coma and death. • Chlordiazepoxide can make you sleepy or dizzy, and can slow your thinking and motor skills. o Do not drive, operate heavy machinery, or do other dangerous activities until you know how chlordiazepoxide affects you. o Do not drink alcohol or take other drugs that may make you sleepy or dizzy while taking chlordiazepoxide without first talking to your healthcare provider.

When taken with alcohol or drugs that cause sleepiness or dizziness, chlordiazepoxide may make your sleepiness or dizziness much worse. o Do not take more chlordiazepoxide than prescribed. What is chlordiazepoxide? • Chlordiazepoxide is a prescription medicine used: o to treat anxiety disorders o for the short-term relief of the symptoms of anxiety o to treat withdrawal symptoms of acute alcoholism o preoperatively to treat apprehension and anxiety • Chlordiazepoxide is a federal controlled substance (C-IV) because it can be abused or lead to dependence.

Keep chlordiazepoxide in a safe place to prevent misuse and abuse. Selling or giving away chlordiazepoxide may harm others, and is against the law. Tell your healthcare provider if you have abused or been dependent on alcohol, prescription medicines or street drugs. • It is not known if chlordiazepoxide is safe and effective in children under 6 years of age. • It is not known if chlordiazepoxide is safe and effective for use for longer than 4 months.

Do not take chlordiazepoxide if you are allergic to chlordiazepoxide or to any of the ingredients in Chlordiazepoxide Hydrochloride Capsules. See the end of this Medication Guide for a complete list of ingredients in Chlordiazepoxide Hydrochloride Capsules. Before you take chlordiazepoxide Hydrochloride, tell your healthcare provider about all of your medical conditions, including if you: • have or have had depression, mood problems, or suicidal thoughts or behavior • have a history of drug or alcohol abuse or addiction • have liver or kidney problems • are pregnant or plan to become pregnant.

Chlordiazepoxide may harm your unborn baby. You and your healthcare provider should decide if you should take chlordiazepoxide while you are pregnant • are breastfeeding or plan to breastfeed. Chlordiazepoxide may pass into your breast milk and may harm your baby.

Talk to your healthcare provider about the best way to feed your baby if you take chlordiazepoxide . Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking chlordiazepoxide with certain other medicines can cause side effects or affect how well chlordiazepoxide or the other medicines work.

Do not start or stop other medicines without talking to your healthcare provider. How should I take chlordiazepoxide ? • Take chlordiazepoxide exactly as your healthcare provider tells you to take it. Your healthcare provider will tell you how much chlordiazepoxide to take and when to take it. • If you take too much chlordiazepoxide, call your healthcare provider or go to the nearest hospital emergency room right away.

What should I avoid while taking chlordiazepoxide ? • Chlordiazepoxide can cause you to be drowsy. Do not drive a car or operate heavy machinery until you know how chlordiazepoxide affects you. • You should not drink alcohol while taking chlordiazepoxide. Drinking alcohol can increase your chances of having serious side effects.

What are the possible side effects of chlordiazepoxide ? Chlordiazepoxide may cause serious side effects, including: • See “What is the most important information I should know about chlordiazepoxide ?” •… [Excerpted — this section continues on DailyMed.]

⚠️ Precautions 1 words ▾

PRECAUTIONS:

🔒 Drug Abuse and Dependence 4 words ▾

DRUG ABUSE AND DEPENDENCE:

📄 Package Label / Principal Display Panel 6 words ▾

PRINCIPAL DISPLAY PANEL CHLORIAZEPOXIDE 25mg

593-30

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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Who lists this product with the FDA?
DIRECT RX 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.
← 61919-0588-30 · DIRECT 61919-0605-30 · DirectRX →
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.