cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler rising pharma holdings, inc.
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 2 mg/5mL

Manufacturer
Rising Pharma Holdings, Inc.

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
866021
UPC
0364980504485
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 ANDA040668 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (64980-504-48)
source: ndc

Packages (1)

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": "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"}