cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-236
Product ID 62135-236_f33fcf42-0b48-eed9-e053-2995a90abefb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088212
Listing Expiration 2026-12-31
Marketing Start 1983-05-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135236
Hyphenated Format 62135-236

Supplemental Identifiers

RxCUI
866144
UPC
0362135236908
UNII
NJ82J0F8QC

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cyproheptadine hydrochloride (source: ndc)
Generic Name cyproheptadine hydrochloride (source: ndc)
Application Number ANDA088212 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (62135-236-90)
source: ndc

Packages (1)

62135-236-90 90 TABLET in 1 BOTTLE (62135-236-90)

Ingredients (1)

cyproheptadine hydrochloride (4 mg/1)

Linked Drug Pages (1)

Cyproheptadine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f33fcf42-0b48-eed9-e053-2995a90abefb", "openfda": {"upc": ["0362135236908"], "unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["029ed3b6-175e-4a1a-81ed-350bff5f6167"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-236-90)", "package_ndc": "62135-236-90", "marketing_start_date": "20230105"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "62135-236_f33fcf42-0b48-eed9-e053-2995a90abefb", "dosage_form": "TABLET", "product_ndc": "62135-236", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA088212", "marketing_category": "ANDA", "marketing_start_date": "19830526", "listing_expiration_date": "20261231"}