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Dicyclomine hydrochloride 20 mg Tablet, 20-count — NDC 50090-8090-2 (Billing 50090-8090-02)

by A-S Medication Solutions · 20 TABLET in 1 BOTTLE

This is a package of 20 tablets of Dicyclomine hydrochloride 20 mg Tablet from A-S Medication Solutions, marketed since May 2024 and currently FDA-listed.

NDC 50090-8090-02
🏷️ FDA NDC (as labeled) 50090-8090-2 billing pads the package segment with a zero
This package
Contains20-count Pack sizes3 compare ↓
Product page 50090-8090-00 Also comes in: 30 tablets 50090-8090-0 90 tablets 50090-8090-8
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

⚠️
Other active recalls for Dicyclomine Hydrochloride (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 · Jul 23, 2026 — shortfill; reports of empty capsules. (Aurobindo Pharma USA Inc) · FDA recall D-0733-2026
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) 50090-8090-2
Product NDC 50090-8090
11-digit billing NDC 50090809002
Application # ANDA217566
SPL Set ID 486f5132-538b-4875-9f40-e70f52bd1f8f
Established class (EPC) Anticholinergic
Mechanism of action Cholinergic Antagonists
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-05-07
Route ORAL
Dosage form TABLET
Substance DICYCLOMINE HYDROCHLORIDE
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 50090-8090-2 — 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 → 50090-8090-02. 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 treats functional bowel/irritable bowel syndrome. It helps calm the spasms and cramping in your intestines.
  • The capsules, tablets and solution are taken by mouth, generally four times a day. Your prescriber may adjust the amount after a week or so. If you miss a dose, just carry on with...
  • Dry mouth, dizziness and blurred vision are the most common. Nausea, drowsiness, weakness and nervousness can happen too. Be careful driving until you know how it affects you.
  • Call if you feel confused, see or hear things that aren't there, have a racing heartbeat, or can't pass urine. Also call if you overheat without sweating or have diarrhea with a co...
📖 Read our full Dicyclomine 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 · 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.
Try another pack size: 30 tablets 90 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
50090-8090-00 50090-8090-0 Main listing 30 TABLET in 1 BOTTLE 2026-09-23 — Active
50090-8090-02 You're viewing this 20 TABLET in 1 BOTTLE 2026-09-23 — Active
50090-8090-08 50090-8090-8 90 TABLET in 1 BOTTLE 2026-09-23 — Active

You're viewing the smallest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 20-count package — 20 tablet in 1 bottle.
How does this package differ from NDC 50090-8090-00?
Both are Dicyclomine hydrochloride 20 mg Tablet — the drug itself is identical. This page's package is the 20-count one, while NDC 50090-8090-00 is the 30 tablets package.
What NDC number is used to bill for this package of Dicyclomine hydrochloride 20 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
Dicyclomine hydrochloride 20 mg 00832-6052-10 Upsher-Smith 1000 tablets $0.056 AB Discontinued —
Dicyclomine 20 mg 00143-1227-01 Hikma 100 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 59651-0720-01 Aurobindo 100 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 73473-0902-01 Solaris 100 tablets $0.059 AB Availability likely —
Dicyclomine hydrochloride 20 mg 16571-0259-01 Rising 100 tablets $0.059 AB Availability likely —
Dicyclomine hydrochloride 20 mg 72888-0119-00 Advagen 1000 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 00591-0795-01 Actavis 100 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 24979-0200-01 Upsher-Smith 100 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 62135-0428-12 Chartwell 120 tablets $0.059 AB Availability likely —
Dicyclomine hydrochloride 20 mg 31722-0079-01 Camber 100 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 69452-0311-20 Bionpharma 100 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 00904-6988-61 Major 100 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 60687-0380-01 American 100 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 00527-1282-01 Lannett 100 tablets $0.059 AB Availability likely —
Dicyclomine Hydrochloride 20 mg 63187-0784-15 Proficient 15 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 71610-0209-09 Aphena 9000 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 72162-1077-03 Bryant 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 82868-0103-30 Northwind 30 tablets — AB FDA listed —
Dicyclomine 20 mg 68071-3782-03 NuCare 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 70518-3917-00 REMEDYREPACK 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 87441-0007-01 Unit 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 43063-0045-04 PD-Rx 4 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 60760-0802-30 St. 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 63187-0410-15 Proficient 15 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 67296-2154-01 Redpharm 15 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 71335-0425-01 Bryant 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 71335-2341-01 Bryant 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 72162-2612-00 Bryant 1000 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 67046-1164-03 Coupler 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 68788-7811-02 Preferred 20 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 68071-3555-03 NuCare 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 68071-3645-03 NuCare 30 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 68071-3916-06 NuCare 6 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 68071-3648-06 NuCare 100 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 68788-8751-02 Preferred 20 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 71335-2506-00 Bryant 10 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 68071-3885-02 NuCare 20 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 68071-5298-03 NuCare 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 70518-4393-00 REMEDYREPACK 30 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 00615-8622-39 NCS 30 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 50090-7732-00 A-S 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 50090-7882-00 A-S 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 51407-0821-12 Golden 120 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 51655-0257-26 Northwind 90 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 51655-0940-26 Northwind 90 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 60760-0665-30 St. 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 68071-3255-01 NuCare 10 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 70518-1767-00 REMEDYREPACK 30 tablets — AB Discontinued —
Dicyclomine Hydrochloride 20 mg 72789-0539-01 PD-Rx 100 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 60760-0931-30 St. 30 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 67296-2175-01 Redpharm 10 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 67296-2226-05 Bionpharma 56 tablets — AB Discontinued —
Dicyclomine hydrochloride 20 mg 72789-0466-01 PD-Rx 100 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 50090-1577-00 A-S 30 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 51655-0548-26 Northwind 90 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 68071-3606-06 NuCare 6 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 68071-4782-01 NuCare 10 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 50090-7309-00 A-S 30 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 67296-2142-01 Redpharm 10 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 70518-4555-00 REMEDYREPACK 180 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 71335-2226-01 Bryant 30 tablets — AB FDA listed —
Dicyclomine Hydrochloride 20 mg 67296-2294-04 Redpharm 15 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 68788-4146-03 Preferred 30 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mg 67296-2311-02 Redpharm 15 tablets — AB FDA listed —
dicyclomine hydrochloride 20 mg 00054-0885-25 Hikma 100 tablets — AB FDA listed —
Dicyclomine hydrochloride 20 mgthis 50090-8090-02 A-S 20 tablets — 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

🏛️
2024
On the market since
May 2024
📍
2026
Currently FDA-listed
2 years 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.

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

LabelerA-S Medication Solutions
Application holderANNORA PHARMA PRIVATE LTD
FDA applicationANDA217566 (ANDA)
Labeler code50090
First marketedMay 2024
Product typeHuman Prescription Drug
Portfolio2,811 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 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 A-S Medication Solutions. 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 2 other package presentations of this same product, including 30 tablets (50090-8090-00), 90 tablets (50090-8090-08). 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?
A-S Medication Solutions 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.
← 50090-8089-00 · A-S 50090-8092-00 · A-S →
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.