NDC codes

FDA NDC Directory
Product NDC (as listed)50090-5491Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-5491Add 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
50090-5491-1500905491015009054910130 TABLET in 1 BOTTLE (50090-5491-1)Marketed from Mar 16, 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)
Cyproheptadine Hydrochloride
Generic name (nonproprietary)
cyproheptadine hydrochloride
Active ingredients
Cyproheptadine hydrochloride — 4 mg/1
Dosage form
Tablet
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206553
Marketing start
Listing expires
Identifiers
Product ID 50090-5491_28b91c2a-e33a-4b09-8636-4c53ea6f1358SPL ID 28b91c2a-e33a-4b09-8636-4c53ea6f1358SPL set ID 7e156e5e-e4cc-420b-8f1a-af123eaa9156RxCUI 866144UNII NJ82J0F8QC

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

N450090549101 followed by a unit qualifier and the quantity

Package 50090-5491-01. 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 Perennial and seasonal allergic rhinitis Vasomotor rhinitis Allergic conjunctivitis due to inhalant allergens and foods Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Amelioration of allergic reactions to blood or plasma Cold urticaria Dermatographism As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-5491

What is NDC 50090-5491?
50090-5491 is the product NDC for Cyproheptadine Hydrochloride, Cyproheptadine hydrochloride 4 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cyproheptadine Hydrochloride.
What is the active ingredient?
Cyproheptadine hydrochloride.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cyproheptadine Hydrochloride?
34 other product NDCs are listed under this name. See all Cyproheptadine 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 Cyproheptadine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 2 mg/1TabletOralPANGEA PHARMACEUTICALS, LLC81279-12981279-0129-3081279-0129-60
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 4 mg/1TabletOralTRUPHARMA, LLC52817-41552817-0415-1052817-0415-50
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 4 mg/1TabletOralREMEDYREPACK INC.70518-466770518-4667-00
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 4 mg/1TabletOralAvPAK50268-20150268-0201-15
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 2 mg/5mLSolutionOralAtlantic Biologicals Corp.17856-118517856-1185-0117856-1185-02
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 2 mg/5mLSolutionOralQUAGEN PHARMACEUTICALS LLC70752-18570752-0185-12
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 4 mg/1TabletOralREMEDYREPACK INC.70518-351770518-3517-00
Cyproheptadine HydrochlorideCyproheptadine 2 mg/5mLSolutionOralPatrin Pharma, Inc.39328-54439328-0544-16
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 4 mg/1TabletOralRising Pharma Holdings, Inc.16571-80516571-0805-0116571-0805-10
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 2 mg/5mLSyrupOralTris Pharma Inc27808-09927808-0099-01

All 35 Cyproheptadine Hydrochloride NDCs

Other NDCs under ANDA 206553

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

FDA NDC Directory listings under ANDA 206553
ProductStrengthForm · routeLabelerProduct NDC
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 4 mg/1TabletOralQPharma Inc42708-177
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 4 mg/1TabletOralTRUPHARMA, LLC52817-210
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 4 mg/1TabletOralTRUPHARMA, LLC52817-415
Cyproheptadine HydrochlorideCyproheptadine hydrochloride 4 mg/1TabletOralBryant Ranch Prepack71335-0211

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