Package 62135-236-90

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-236-90
Digits Only 6213523690
Product NDC 62135-236
Product ID 62135-236_f33fcf42-0b48-eed9-e053-2995a90abefb
Description

90 TABLET in 1 BOTTLE (62135-236-90)

Marketing

Marketing Status
Marketed Since 2023-01-05
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": "f33fcf42-0b48-eed9-e053-2995a90abefb", "openfda": {"upc": ["0362135236908"], "unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["029ed3b6-175e-4a1a-81ed-350bff5f6167"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-236-90)", "package_ndc": "62135-236-90", "marketing_start_date": "20230105"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "62135-236_f33fcf42-0b48-eed9-e053-2995a90abefb", "dosage_form": "TABLET", "product_ndc": "62135-236", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA088212", "marketing_category": "ANDA", "marketing_start_date": "19830526", "listing_expiration_date": "20261231"}