cyproheptadine
Generic: cyproheptadine hydrochloride
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
cyproheptadine
Generic Name
cyproheptadine hydrochloride
Labeler
chartwell rx, llc
Dosage Form
SYRUP
Routes
Active Ingredients
cyproheptadine hydrochloride 2 mg/5mL
Manufacturer
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
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 2 mg/5mL
Packaging
- 473 mL in 1 BOTTLE (62135-949-47)
- 946 mL in 1 BOTTLE (62135-949-94)
Packages (2)
Ingredients (1)
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"}