What is NDC 72888-198?

72888-198 is the product NDC for Dicyclomine hydrochloride, Dicyclomine hydrochloride 40 mg/1 tablet, listed with the FDA by Advagen Pharma Ltd.,. It has 5 package NDCs, shown above in 10- and 11-digit form.

Advagen Pharma Ltd.,, NDC labeler code 72888. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Dicyclomine hydrochloride?

126 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dicyclomine hydrochloride NDC 72888-198

NDC codes

FDA NDC Directory

Product NDC (as listed)72888-198Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72888-0198Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
72888-198-00	7288801980072888019800	1000 TABLET in 1 BOTTLE (72888-198-00)Marketed from Mar 25, 2025
72888-198-01	7288801980172888019801	100 TABLET in 1 BOTTLE (72888-198-01)Marketed from Mar 25, 2025
72888-198-05	7288801980572888019805	500 TABLET in 1 BOTTLE (72888-198-05)Marketed from Mar 25, 2025
72888-198-12	7288801981272888019812	120 TABLET in 1 BOTTLE (72888-198-12)Marketed from Mar 25, 2025
72888-198-30	7288801983072888019830	30 TABLET in 1 BOTTLE (72888-198-30)Marketed from Feb 17, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Dicyclomine hydrochloride
Generic name (nonproprietary): dicyclomine hydrochloride
Active ingredients: Dicyclomine hydrochloride — 40 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Advagen Pharma Ltd.,NDC labeler code 72888
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216736
Marketing start: Mar 25, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Cholinergic Antagonists (Mechanism)
Identifiers: Product ID 72888-198_4b7e07c5-f687-74a5-e063-6294a90aa7efSPL ID 4b7e07c5-f687-74a5-e063-6294a90aa7efSPL set ID b4331e24-58af-45fb-a25b-9eb8270f83f7RxCUI 991086, 2719470UNII CQ903KQA31UPC 0372888198309, 0372888119014, 0372888198002, 0372888198057, 0372888198125, 0372888119304, 0372888119007, 0372888119052, 0372888198019
Pharmacologic class: Anticholinergic

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472888019800 followed by a unit qualifier and the quantity

Package 72888-0198-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Feb 23, 2026.

Indications (excerpt from the label)

Dicyclomine hydrochloride tablets are indicated for the treatment of patients with functional bowel/irritable bowel syndrome. Dicyclomine hydrochloride is an antispasmodic and anticholinergic (antimuscarinic) agent indicated for the treatment of functional bowel/irritable bowel syndrome ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72888-198

What is NDC 72888-198?: 72888-198 is the product NDC for Dicyclomine hydrochloride, Dicyclomine hydrochloride 40 mg/1 tablet, listed with the FDA by Advagen Pharma Ltd.,. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Dicyclomine hydrochloride.
What is the active ingredient?: Dicyclomine hydrochloride.
Who is the labeler?: Advagen Pharma Ltd.,, NDC labeler code 72888. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dicyclomine hydrochloride?: 126 other product NDCs are listed under this name. See all Dicyclomine hydrochloride NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Dicyclomine hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
dicyclomine hydrochloride	Dicyclomine hydrochloride 10 mg/1	CapsuleOral	Hikma Pharmaceuticals USA Inc.	0054-0883	00054-0883-2500054-0883-31
dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Hikma Pharmaceuticals USA Inc.	0054-0885	00054-0885-2500054-0885-31
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4146	68788-4146-03
Dicyclomine hydrochloride	Dicyclomine hydrochloride 10 mg/1	CapsuleOral	Advagen Pharma Ltd.,	72888-105	72888-0105-0072888-0105-0172888-0105-05+1 more
Dicyclomine Hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-007	87441-0007-01
Dicyclomine Hydrochloride	Dicyclomine hydrochloride 10 mg/1	CapsuleOral	Coupler LLC	67046-1258	67046-1258-03
Dicyclomine Hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Coupler LLC	67046-1164	67046-1164-03
Dicyclomine Hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Northwind Health Company, LLC	82868-103	82868-0103-30
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4555	70518-4555-00
Dicyclomine Hydrochloride	Dicyclomine hydrochloride 10 mg/1	CapsuleOral	PD-Rx Pharmaceuticals, Inc.	72789-522	72789-0522-0172789-0522-2072789-0522-28+5 more

All 127 Dicyclomine hydrochloride NDCs

Other NDCs under ANDA 216736

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 216736
Product	Strength	Form · route	Labeler	Product NDC
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8622
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	A-S Medication Solutions	50090-7732
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Northwind Health Company, LLC	51655-548
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-802
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Redpharm Drug	67296-2142
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Redpharm Drug	67296-2175
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-2226
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-466
Dicyclomine hydrochloride	Dicyclomine hydrochloride 20 mg/1	TabletOral	Advagen Pharma Ltd.,	72888-119
Dicyclomine hydrochloride	Dicyclomine hydrochloride 40 mg/1	TabletOral	Trifluent Pharma, LLC	73352-119