cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

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

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler patrin pharma, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

cyproheptadine 2 mg/5mL

Manufacturer
Patrin Pharma, Inc.

Identifiers & Regulatory

Product NDC 39328-544
Product ID 39328-544_fcdc36f7-1523-46dc-a976-c3d150fae843
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209108
Listing Expiration 2026-12-31
Marketing Start 2022-02-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 39328544
Hyphenated Format 39328-544

Supplemental Identifiers

RxCUI
866021
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 (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 (39328-544-16)
source: ndc

Packages (1)

Ingredients (1)

cyproheptadine (2 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fcdc36f7-1523-46dc-a976-c3d150fae843", "openfda": {"unii": ["2YHB6175DO"], "rxcui": ["866021"], "spl_set_id": ["81d9523f-f945-4410-8b71-8b5fea48a3da"], "manufacturer_name": ["Patrin Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, GLASS (39328-544-16)", "package_ndc": "39328-544-16", "marketing_start_date": "20220215"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "39328-544_fcdc36f7-1523-46dc-a976-c3d150fae843", "dosage_form": "SOLUTION", "product_ndc": "39328-544", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "Patrin Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE", "strength": "2 mg/5mL"}], "application_number": "ANDA209108", "marketing_category": "ANDA", "marketing_start_date": "20220215", "listing_expiration_date": "20261231"}