NDC codes

FDA NDC Directory
Product NDC (as listed)71872-7242Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71872-7242Add 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
71872-7242-1718727242011 CUP, UNIT-DOSE in 1 BAG (71872-7242-1) / 10 mL in 1 CUP, UNIT-DOSEMarketed from Mar 1, 2021

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)
Diphenhydramine Hydrochloride
Generic name (nonproprietary)
diphenhydramine hydrochloride
Active ingredients
Diphenhydramine hydrochloride — 25 mg/10mL
Dosage form
Solution
Route
Oral
Labeler
Medical Purchasing Solutions, LLCNDC labeler code 71872
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 087513
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 71872-7242_fa59581e-a76f-d735-e053-6294a90acd1aSPL ID fa59581e-a76f-d735-e053-6294a90acd1aSPL set ID bf7ab250-38b0-ba29-e053-2a95a90a8f32RxCUI 1049906UNII TC2D6JAD40
Pharmacologic class
Histamine-1 Receptor Antagonist

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

N471872724201 followed by a unit qualifier and the quantity

Package 71872-7242-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Diphenhydramine hydrochloride in the oral form is effective for the following indications: Antihistaminic For allergic conjunctivitis due to foods; mild, uncomplicated allergic skin manifestations of urticaria and angioedema; amelioration of allergic reactions to blood or plasma; dermatographism; as therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. Motion Sickness For active and prophylactic treatment of motion sickness. Antiparkinsonism For parkinsonism (including drug-induced) in the elderly unable to tolerate more potent agents; mild cases of parkinsonism (including drug-induc…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71872-7242

What is NDC 71872-7242?
71872-7242 is the product NDC for Diphenhydramine Hydrochloride, Diphenhydramine hydrochloride 25 mg/10mL solution, listed with the FDA by Medical Purchasing Solutions, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Diphenhydramine Hydrochloride.
What is the active ingredient?
Diphenhydramine hydrochloride.
Who is the labeler?
Medical Purchasing Solutions, LLC, NDC labeler code 71872. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Diphenhydramine Hydrochloride?
78 other product NDCs are listed under this name. See all Diphenhydramine 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 Diphenhydramine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Diphenhydramine HydrochlorideDiphenhydramine hydrochloride 25 mg/1TabletOralCardinal Health 107, LLC55154-158955154-1589-00
Diphenhydramine HydrochlorideDiphenhydramine hydrochloride 25 mg/1Tablet, Film coatedOralHealth Pharma USA LLC71679-30871679-0308-00
Diphenhydramine hydrochlorideDiphenhydramine hydrochloride 12.5 mg/5mLSolutionOralCamber Pharmaceuticals, Inc.31722-60031722-0600-1131722-0600-31
Diphenhydramine hydrochlorideDiphenhydramine hydrochloride 25 mg/10mLSolutionOralCamber Pharmaceuticals, Inc.31722-60131722-0601-31
Diphenhydramine HydrochlorideDiphenhydramine hydrochloride 50 mg/mLInjectionIntramuscular, IntravenousREMEDYREPACK INC.70518-453670518-4536-00
Diphenhydramine HydrochlorideDiphenhydramine hydrochloride 50 mg/mLInjectionIntramuscular, IntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-26323155-0263-31
Diphenhydramine HydrochlorideDiphenhydramine hydrochloride 50 mg/mLInjectionIntramuscular, IntravenousMicro Labs Limited42571-51142571-0511-56
Diphenhydramine hydrochlorideDiphenhydramine hydrochloride 50 mg/mLInjectionIntramuscular, IntravenousREMEDYREPACK INC.70518-445570518-4455-00
Diphenhydramine HydrochlorideDiphenhydramine hydrochloride 50 mg/1Capsule, Liquid filledOralProdose, Inc.68210-505768210-5057-01
Diphenhydramine HydrochlorideDiphenhydramine hydrochloride 50 mg/mLInjectionIntramuscular, IntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-26423155-0264-41

All 79 Diphenhydramine Hydrochloride NDCs

Other NDCs under ANDA 087513

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

FDA NDC Directory listings under ANDA 087513
ProductStrengthForm · routeLabelerProduct NDC
Diphenhydramine HCLdiphenhydramine hydrochlorideDiphenhydramine hydrochloride 12.5 mg/5mLSolutionOralRedmont Pharmaceuticals, LLC71741-511
Diphenhydramine HydrochlorideDiphenhydramine hydrochloride 12.5 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-0489
Diphenhydramine HydrochlorideDiphenhydramine hydrochloride 25 mg/10mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-0978

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