What is NDC 62135-236?

62135-236 is the product NDC for Cyproheptadine Hydrochloride, Cyproheptadine hydrochloride 4 mg/1 tablet, listed with the FDA by Chartwell RX, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Chartwell RX, LLC, NDC labeler code 62135. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cyproheptadine Hydrochloride NDC 62135-236

NDC codes

FDA NDC Directory

Product NDC (as listed)62135-236Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62135-0236Add 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
62135-236-90	6213502369062135023690	90 TABLET in 1 BOTTLE (62135-236-90)Marketed from Jan 5, 2023

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): Cyproheptadine Hydrochloride
Generic name (nonproprietary): cyproheptadine hydrochloride
Active ingredients: Cyproheptadine hydrochloride — 4 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Chartwell RX, LLCNDC labeler code 62135
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 088212
Marketing start: May 26, 1983
Listing expires: Dec 31, 2026
Identifiers: Product ID 62135-236_f33fcf42-0b48-eed9-e053-2995a90abefbSPL ID f33fcf42-0b48-eed9-e053-2995a90abefbSPL set ID 029ed3b6-175e-4a1a-81ed-350bff5f6167RxCUI 866144UNII NJ82J0F8QCUPC 0362135236908

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

N462135023690 followed by a unit qualifier and the quantity

Package 62135-0236-90. 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 Jan 27, 2023.

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 62135-236

What is NDC 62135-236?: 62135-236 is the product NDC for Cyproheptadine Hydrochloride, Cyproheptadine hydrochloride 4 mg/1 tablet, listed with the FDA by Chartwell RX, LLC. 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?: Chartwell RX, LLC, NDC labeler code 62135. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Cyproheptadine Hydrochloride	Cyproheptadine hydrochloride 2 mg/1	TabletOral	PANGEA PHARMACEUTICALS, LLC	81279-129	81279-0129-3081279-0129-60
Cyproheptadine Hydrochloride	Cyproheptadine hydrochloride 4 mg/1	TabletOral	TRUPHARMA, LLC	52817-415	52817-0415-1052817-0415-50
Cyproheptadine Hydrochloride	Cyproheptadine hydrochloride 4 mg/1	TabletOral	REMEDYREPACK INC.	70518-4667	70518-4667-00
Cyproheptadine Hydrochloride	Cyproheptadine hydrochloride 4 mg/1	TabletOral	AvPAK	50268-201	50268-0201-15
Cyproheptadine Hydrochloride	Cyproheptadine hydrochloride 2 mg/5mL	SolutionOral	Atlantic Biologicals Corp.	17856-1185	17856-1185-0117856-1185-02
Cyproheptadine Hydrochloride	Cyproheptadine hydrochloride 2 mg/5mL	SolutionOral	QUAGEN PHARMACEUTICALS LLC	70752-185	70752-0185-12
Cyproheptadine Hydrochloride	Cyproheptadine hydrochloride 4 mg/1	TabletOral	REMEDYREPACK INC.	70518-3517	70518-3517-00
Cyproheptadine Hydrochloride	Cyproheptadine 2 mg/5mL	SolutionOral	Patrin Pharma, Inc.	39328-544	39328-0544-16
Cyproheptadine Hydrochloride	Cyproheptadine hydrochloride 4 mg/1	TabletOral	Rising Pharma Holdings, Inc.	16571-805	16571-0805-0116571-0805-10
Cyproheptadine Hydrochloride	Cyproheptadine hydrochloride 2 mg/5mL	SyrupOral	Tris Pharma Inc	27808-099	27808-0099-01

All 35 Cyproheptadine Hydrochloride NDCs