cyproheptadine hydrochloride solution (58657-697)

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride solution

Generic Name cyproheptadine hydrochloride

Labeler method pharmaceuticals, llc

Dosage Form SOLUTION

Routes

ORAL

Active Ingredients

cyproheptadine 2 mg/5mL

Manufacturer

Method Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 58657-697

Product ID 58657-697_41b48ab2-962e-790a-e063-6394a90a6106

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA209108

Listing Expiration 2026-12-31

Marketing Start 2024-06-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58657697

Hyphenated Format 58657-697

Supplemental Identifiers

RxCUI

866021

UPC

0358657697167

UNII

2YHB6175DO

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 solution (source: ndc)

Generic Name cyproheptadine hydrochloride (source: ndc)

Application Number ANDA209108 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

2 mg/5mL

source: ndc

Packaging

473 mL in 1 BOTTLE, GLASS (58657-697-16)

source: ndc

Packages (1)

58657-697-16 473 mL in 1 BOTTLE, GLASS (58657-697-16)

Ingredients (1)

cyproheptadine (2 mg/5mL)

Linked Drug Pages (1)

cyproheptadine hydrochloride solution ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "41b48ab2-962e-790a-e063-6394a90a6106", "openfda": {"upc": ["0358657697167"], "unii": ["2YHB6175DO"], "rxcui": ["866021"], "spl_set_id": ["1acfd050-6c07-a269-e063-6394a90a77e8"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, GLASS (58657-697-16)", "package_ndc": "58657-697-16", "marketing_start_date": "20240615"}], "brand_name": "cyproheptadine hydrochloride solution", "product_id": "58657-697_41b48ab2-962e-790a-e063-6394a90a6106", "dosage_form": "SOLUTION", "product_ndc": "58657-697", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Method Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "cyproheptadine hydrochloride solution", "active_ingredients": [{"name": "CYPROHEPTADINE", "strength": "2 mg/5mL"}], "application_number": "ANDA209108", "marketing_category": "ANDA", "marketing_start_date": "20240615", "listing_expiration_date": "20261231"}