What is NDC 51079-375?

51079-375 is the product NDC for Chlordiazepoxide Hydrochloride, Chlordiazepoxide hydrochloride 10 mg/1 capsule, listed with the FDA by Mylan Institutional Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Mylan Institutional Inc., NDC labeler code 51079. 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 Hydrochloride?

27 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Chlordiazepoxide Hydrochloride NDC 51079-375

NDC codes

FDA NDC Directory

Product NDC (as listed)51079-375Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51079-0375Add 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
51079-375-20	51079037520	100 BLISTER PACK in 1 CARTON (51079-375-20) / 1 CAPSULE in 1 BLISTER PACK (51079-375-01)Marketed from May 26, 2022

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): Chlordiazepoxide Hydrochloride
Generic name (nonproprietary): chlordiazepoxide hydrochloride
Active ingredients: Chlordiazepoxide hydrochloride — 10 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Mylan Institutional Inc.NDC labeler code 51079
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 083116
Marketing start: May 26, 2022
Listing expires: Dec 31, 2026
DEA schedule: CIV
Other FDA classes: Benzodiazepines (Chemical structure)
Identifiers: Product ID 51079-375_4358ac27-671d-8c3d-e063-6394a90ae79fSPL ID 4358ac27-671d-8c3d-e063-6394a90ae79fSPL set ID 68c7d8a7-08b3-4a1a-acbd-09bbe67b8d4aRxCUI 905369, 905495, 905516UNII MFM6K1XWDK
Pharmacologic class: 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

N451079037520 followed by a unit qualifier and the quantity

Package 51079-0375-20. 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 11, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Chlordiazepoxide HCl capsules are indicated for the management of anxiety disorders or for the short term relief of symptoms of anxiety, withdrawal symptoms of acute alcoholism, and preoperative apprehension and anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic. The effectiveness of chlordiazepoxide HCl capsules in long term use, that is, more than 4 months, has not been assessed by systematic clinical studies. The physician should periodically reassess the usefulness of the drug for the individual patient.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51079-375

What is NDC 51079-375?: 51079-375 is the product NDC for Chlordiazepoxide Hydrochloride, Chlordiazepoxide hydrochloride 10 mg/1 capsule, listed with the FDA by Mylan Institutional Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Chlordiazepoxide Hydrochloride.
What is the active ingredient?: Chlordiazepoxide hydrochloride.
Who is the labeler?: Mylan Institutional Inc., NDC labeler code 51079. 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 Hydrochloride?: 27 other product NDCs are listed under this name. See all Chlordiazepoxide 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 Chlordiazepoxide Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 10 mg/1	CapsuleOral	Coupler LLC	67046-0909	67046-0909-03
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 25 mg/1	CapsuleOral	Unit Dose Solutions, Inc.	87441-015	87441-0015-01
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 25 mg/1	CapsuleOral	Couper LLC	67046-0910	67046-0910-03
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 10 mg/1	CapsuleOral	Safecor Health, LLC	48433-019	48433-0019-20
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 25 mg/1	CapsuleOral	Safecor Health, LLC	48433-020	48433-0020-20
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 25 mg/1	CapsuleOral	American Health Packaging	60687-807	60687-0807-01
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 25 mg/1	CapsuleOral	Mylan Institutional Inc.	51079-141	51079-0141-20
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 5 mg/1	Capsule, Gelatin coatedOral	Epic Pharma, LLC	42806-564	42806-0564-01
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 10 mg/1	Capsule, Gelatin coatedOral	Epic Pharma, LLC	42806-565	42806-0565-01
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 25 mg/1	Capsule, Gelatin coatedOral	Epic Pharma, LLC	42806-566	42806-0566-01

All 28 Chlordiazepoxide Hydrochloride NDCs

Other NDCs under ANDA 083116

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

FDA NDC Directory listings under ANDA 083116
Product	Strength	Form · route	Labeler	Product NDC
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 10 mg/1	CapsuleOral	Teva Pharmaceuticals USA, Inc.	0555-0033
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 10 mg/1	CapsuleOral	Safecor Health, LLC	48433-019
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 10 mg/1	CapsuleOral	Clinical Solutions Wholesale, LLC	58118-1033
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 10 mg/1	CapsuleOral	Coupler LLC	67046-0909
Chlordiazepoxide Hydrochloride	Chlordiazepoxide hydrochloride 10 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-1752