cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyproheptadine hydrochloride
Generic Name cyproheptadine hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyproheptadine hydrochloride 4 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-102
Product ID 72789-102_4af611bc-838d-98d2-e063-6294a90a74d8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206676
Listing Expiration 2027-12-31
Marketing Start 2020-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789102
Hyphenated Format 72789-102

Supplemental Identifiers

RxCUI
866144
UPC
0372789102306
UNII
NJ82J0F8QC

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 ANDA206676 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-102-01)
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-102-30)
source: ndc

Packages (2)

72789-102-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-102-01) 72789-102-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-102-30)

Ingredients (1)

cyproheptadine hydrochloride (4 mg/1)

Linked Drug Pages (1)

Cyproheptadine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4af611bc-838d-98d2-e063-6294a90a74d8", "openfda": {"upc": ["0372789102306"], "unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["03e69414-8a25-4ed8-b7ac-16445b879b1f"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-102-01)", "package_ndc": "72789-102-01", "marketing_start_date": "20230710"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-102-30)", "package_ndc": "72789-102-30", "marketing_start_date": "20200727"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "72789-102_4af611bc-838d-98d2-e063-6294a90a74d8", "dosage_form": "TABLET", "product_ndc": "72789-102", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA206676", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20271231"}