NDC codes

FDA NDC Directory
Product NDC (as listed)60687-576Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0576Add 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
60687-576-1060687057610606870576103 TRAY in 1 CASE (60687-576-10) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-576-04) / 2.5 mL in 1 CUP, UNIT-DOSE (60687-576-03)Marketed from Jun 15, 2021
60687-576-8660687057686606870576863 TRAY in 1 CASE (60687-576-86) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-576-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-576-40)Marketed from Jun 15, 2021

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)
Midazolam Hydrochloride
Generic name (nonproprietary)
midazolam hydrochloride
Active ingredients
Midazolam hydrochloride — 2 mg/mL
Dosage form
Syrup
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075873
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 60687-576_57afebca-8a3d-c511-e063-6394a90a2cb0SPL ID 57afebca-8a3d-c511-e063-6394a90a2cb0SPL set ID fc93242b-0abf-466a-8413-8a365620ee75RxCUI 422410UNII W7TTW573JJ
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

N460687057610 followed by a unit qualifier and the quantity

Package 60687-0576-10. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Midazolam HCl syrup is indicated for use in pediatric patients for sedation, anxiolysis and amnesia prior to diagnostic, therapeutic or endoscopic procedures or before induction of anesthesia. Midazolam HCl syrup is intended for use in monitored settings only and not for chronic or home use [see WARNINGS ].

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-576

What is NDC 60687-576?
60687-576 is the product NDC for Midazolam Hydrochloride, Midazolam hydrochloride 2 mg/mL syrup, listed with the FDA by American Health Packaging. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Midazolam Hydrochloride.
What is the active ingredient?
Midazolam hydrochloride.
Who is the labeler?
American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Midazolam Hydrochloride?
14 other product NDCs are listed under this name. See all Midazolam 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 Midazolam Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Midazolam HydrochlorideMidazolam hydrochloride 5 mg/mLInjection, SolutionIntramuscular, IntravenousJvet Pharmaceuticals LLC86211-11186211-0111-10
Midazolam HydrochlorideMidazolam hydrochloride 5 mg/mLInjection, SolutionIntramuscular, IntravenousBelcher Pharmaceuticals, LLC62250-11162250-0111-10
Midazolam HydrochlorideMidazolam hydrochloride 5 mg/mLInjection, SolutionIntramuscular, IntravenousHenry Schein, Inc.0404-991600404-9916-0100404-9916-02
Midazolam hydrochlorideMidazolam hydrochloride 1 mg/mLInjection, SolutionIntramuscular, IntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-60023155-0600-41
Midazolam hydrochlorideMidazolam hydrochloride 5 mg/mLInjection, SolutionIntramuscular, IntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-60123155-0601-4123155-0601-42
Midazolam HydrochlorideMidazolam hydrochloride 2 mg/mLSyrupOralPrecision Dose Inc.68094-76268094-0762-62
Midazolam HydrochlorideMidazolam hydrochloride 2 mg/mLSyrupOralPrecision Dose Inc.68094-76468094-0764-62
Midazolam hydrochlorideMidazolam hydrochloride 1 mg/mLInjection, SolutionIntramuscular, IntravenousGland Pharma Limited68083-10668083-0106-01
Midazolam HydrochlorideMidazolam hydrochloride 5 mg/mLInjection, SolutionIntramuscular, IntravenousGland Pharma Limited68083-10868083-0108-0168083-0108-02
Midazolam HydrochlorideMidazolam hydrochloride 1 mg/mLInjection, SolutionIntramuscular, IntravenousA-S Medication Solutions50090-547250090-5472-00

All 15 Midazolam Hydrochloride NDCs

Other NDCs under ANDA 075873

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

FDA NDC Directory listings under ANDA 075873
ProductStrengthForm · routeLabelerProduct NDC
Midazolam HydrochlorideMidazolam hydrochloride 2 mg/mLSyrupOralHikma Pharmaceuticals USA Inc.0054-3566
Midazolam HydrochlorideMidazolam hydrochloride 2 mg/mLSyrupOralPrecision Dose Inc.68094-762
Midazolam HydrochlorideMidazolam hydrochloride 2 mg/mLSyrupOralPrecision Dose Inc.68094-764

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