What is NDC 72162-2436?

72162-2436 is the product NDC for Chlordiazepoxide HCl And Clidinium Bromide, Chlordiazepoxide hydrochloride 5 mg/1; Clidinium bromide 2.5 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Chlordiazepoxide hydrochloride, Clidinium bromide.

Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Chlordiazepoxide HCl And Clidinium Bromide?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Chlordiazepoxide HCl And Clidinium Bromide NDC 72162-2436

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2436Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2436Add 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	Copy
72162-2436-1	72162243601	100 CAPSULE in 1 BOTTLE (72162-2436-1)Marketed from Feb 13, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Chlordiazepoxide HCl And Clidinium Bromide
Generic name (nonproprietary): chlordiazepoxide hcl and clidinium bromide
Active ingredients: Chlordiazepoxide hydrochloride — 5 mg/1Clidinium bromide — 2.5 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215835
Marketing start: Oct 1, 2022
Listing expires: Dec 31, 2026
DEA schedule: CIV
Other FDA classes: Benzodiazepines (Chemical structure)Cholinergic Antagonists (Mechanism)Decreased Parasympathetic Acetylcholine Activity (Physiologic effect)Digestive/GI System Activity Alteration (Physiologic effect)GI Motility Alteration (Physiologic effect)
Identifiers: Product ID 72162-2436_bf5abb7c-5ad5-4817-8d72-0b1ae5a52741SPL ID bf5abb7c-5ad5-4817-8d72-0b1ae5a52741SPL set ID ec7733c5-3aad-496a-8007-5d7596ede630RxCUI 889614UNII MFM6K1XWDK, 91ZQW5JF1Z
Pharmacologic class: Anticholinergic; Benzodiazepine

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

N472162243601 followed by a unit qualifier and the quantity

Package 72162-2436-01. 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 Nov 4, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Chlordiazepoxide hydrochloride and clidinium bromide capsule is indicated to control emotional and somatic factors in gastrointestinal disorders. Chlordiazepoxide hydrochloride and clidinium bromide capsules may also be used as adjunctive therapy in the treatment of peptic ulcer and in the treatment of the irritable bowel syndrome (irritable colon, spastic colon, mucous colitis) and acute enterocolitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2436

What is NDC 72162-2436?: 72162-2436 is the product NDC for Chlordiazepoxide HCl And Clidinium Bromide, Chlordiazepoxide hydrochloride 5 mg/1; Clidinium bromide 2.5 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Chlordiazepoxide HCl And Clidinium Bromide.
What is the active ingredient?: Chlordiazepoxide hydrochloride, Clidinium bromide.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Chlordiazepoxide HCl And Clidinium Bromide?: 1 other product NDC are listed under this name. See all Chlordiazepoxide HCl And Clidinium Bromide 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 Chlordiazepoxide HCl And Clidinium Bromide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Chlordiazepoxide HCl And Clidinium Bromide	Chlordiazepoxide hydrochloride 5 mg/1; Clidinium bromide 2.5 mg/1	CapsuleOral	Micro Labs Limited	42571-381	42571-0381-01

Other NDCs under ANDA 215835

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

FDA NDC Directory listings under ANDA 215835
Product	Strength	Form · route	Labeler	Product NDC
Chlordiazepoxide HCl And Clidinium Bromide	Chlordiazepoxide hydrochloride 5 mg/1; Clidinium bromide 2.5 mg/1	CapsuleOral	Micro Labs Limited	42571-381