cyproheptadine hydrochloride
Generic: cyproheptadine hydrochloride
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
cyproheptadine hydrochloride
Generic Name
cyproheptadine hydrochloride
Labeler
rising pharma holdings, inc.
Dosage Form
SYRUP
Routes
Active Ingredients
cyproheptadine hydrochloride 2 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
64980-504
Product ID
64980-504_9b4845c1-9b59-4809-9247-50565fc4b6fb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040668
Listing Expiration
2026-12-31
Marketing Start
2006-07-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
64980504
Hyphenated Format
64980-504
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 hydrochloride (source: ndc)
Generic Name
cyproheptadine hydrochloride (source: ndc)
Application Number
ANDA040668 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/5mL
Packaging
- 473 mL in 1 BOTTLE (64980-504-48)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9b4845c1-9b59-4809-9247-50565fc4b6fb", "openfda": {"upc": ["0364980504485"], "unii": ["NJ82J0F8QC"], "rxcui": ["866021"], "spl_set_id": ["e2bf4d46-6585-41d9-868c-98603b165d5b"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (64980-504-48)", "package_ndc": "64980-504-48", "marketing_start_date": "20060710"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "64980-504_9b4845c1-9b59-4809-9247-50565fc4b6fb", "dosage_form": "SYRUP", "product_ndc": "64980-504", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "2 mg/5mL"}], "application_number": "ANDA040668", "marketing_category": "ANDA", "marketing_start_date": "20060710", "listing_expiration_date": "20261231"}