cyproheptadine

Generic: cyproheptadine hydrochloride

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

Drug Facts

Product Profile

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

cyproheptadine hydrochloride 2 mg/5mL

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-949
Product ID 62135-949_06fd9a7b-3b04-6e0c-e063-6394a90aba46
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203191
Listing Expiration 2026-12-31
Marketing Start 2017-07-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135949
Hyphenated Format 62135-949

Supplemental Identifiers

RxCUI
866021
UPC
0362135949945
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 (source: ndc)
Generic Name cyproheptadine hydrochloride (source: ndc)
Application Number ANDA203191 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (62135-949-47)
  • 946 mL in 1 BOTTLE (62135-949-94)
source: ndc

Packages (2)

Ingredients (1)

cyproheptadine hydrochloride (2 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "06fd9a7b-3b04-6e0c-e063-6394a90aba46", "openfda": {"upc": ["0362135949945"], "unii": ["NJ82J0F8QC"], "rxcui": ["866021"], "spl_set_id": ["37fe7264-4d45-4d6c-ac13-40fcd1d82351"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (62135-949-47)", "package_ndc": "62135-949-47", "marketing_start_date": "20220713"}, {"sample": false, "description": "946 mL in 1 BOTTLE (62135-949-94)", "package_ndc": "62135-949-94", "marketing_start_date": "20220713"}], "brand_name": "CYPROHEPTADINE", "product_id": "62135-949_06fd9a7b-3b04-6e0c-e063-6394a90aba46", "dosage_form": "SYRUP", "product_ndc": "62135-949", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "2 mg/5mL"}], "application_number": "ANDA203191", "marketing_category": "ANDA", "marketing_start_date": "20170713", "listing_expiration_date": "20261231"}