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Prescription medicine · generic available

Bethanechol chloride

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Bethanechol chloride used for?
The FDA-approved label (Bethanechol Chloride, Amneal Pharmaceuticals of New York LLC, January 29, 2026) says: “Bethanechol chloride tablets are indicated for the treatment of acute postoperative and postpartum nonobstructive (functional) urinary retention and for neurogenic atony of the urinary bladder with retention.” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Bethanechol chloride have a boxed warning?
No. None of the 5 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Bethanechol chloride?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Bethanechol chloride been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Bethanechol chloride?
6 companies list prescription products of Bethanechol chloride in the FDA NDC Directory, including Amneal Pharmaceuticals LLC, Upsher-Smith Laboratories, LLC and Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc..

What Bethanechol chloride is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

Bethanechol chloride tablets are indicated for the treatment of acute postoperative and postpartum nonobstructive (functional) urinary retention and for neurogenic atony of the urinary bladder with retention.

— FDA label: Bethanechol Chloride, Amneal Pharmaceuticals of New York LLC, effective January 29, 2026. Read the full label on DailyMed →

The FDA has 5 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

The label quoted above has no boxed warning.

0 of 5 FDA labels for this medicine have a boxed warning.

Forms and how it is given

Dosage formsTablet
RouteOral
Prescription products22 in the FDA NDC Directory

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Bethanechol chloride, by strength and form
Strength and formGeneric or brandPharmacies pay
bethanechol chloride 10 mg
tablet
Generic $0.1484 per tablet
bethanechol chloride 25 mg
tablet
Generic $0.1787 per tablet
bethanechol chloride 5 mg
tablet
Generic $0.1208 per tablet
bethanechol chloride 50 mg
tablet
Generic $0.2642 per tablet

NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.

Generic approvals (7)

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

RxCUI (RxNorm)857321, 857328, 857336, 857340
SPL set ID of the quoted label16523451-cd3d-4c10-be06-d59a6f12ac68
FDA labels (SPL)5
FDA applications7 ANDA
Active ingredients (FDA)BETHANECHOL

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Bethanechol Chloride, Amneal Pharmaceuticals of New York LLC, effective January 29, 2026; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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