NDC codes

FDA NDC Directory
Product NDC (as listed)70518-0015Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-0015Add 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 NDC11-digit (billing)PackageCopy
70518-0015-07051800150030 CAPSULE in 1 BLISTER PACK (70518-0015-0)Marketed from Nov 23, 2016

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 Hydrochloride
Generic name (nonproprietary)
chlordiazepoxide hydrochloride
Active ingredients
Chlordiazepoxide hydrochloride — 25 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 084769
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 70518-0015_5c01b06a-a4e3-bf44-e063-6394a90a6a65SPL ID 5c01b06a-a4e3-bf44-e063-6394a90a6a65
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

N470518001500 followed by a unit qualifier and the quantity

Package 70518-0015-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 084769

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

FDA NDC Directory listings under ANDA 084769
ProductStrengthForm · routeLabelerProduct NDC
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralREMEDYREPACK INC.70518-0157
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralAmerican Health Packaging60687-807
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-015
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralTeva Pharmaceuticals USA, Inc.0555-0159
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5171
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralPD-Rx Pharmaceuticals, Inc.43063-046
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5256
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralSafecor Health, LLC48433-020
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralClinical Solutions Wholesale, LLC58118-1590
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralCouper LLC67046-0910
Chlordiazepoxide HydrochlorideChlordiazepoxide hydrochloride 25 mg/1CapsuleOralMylan Institutional Inc.51079-141

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