Package 72789-102-30

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-102-30
Digits Only 7278910230
Product NDC 72789-102
Product ID 72789-102_4af611bc-838d-98d2-e063-6294a90a74d8
Description

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

Marketing

Marketing Status
Marketed Since 2020-07-27
Brand cyproheptadine hydrochloride
Generic cyproheptadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cyproheptadine Hydrochloride ndc-match (0.95)

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"}