Package 50268-652-12

Brand: pilocarpine hydrochloride

Generic: pilocarpine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-652-12
Digits Only 5026865212
Product NDC 50268-652
Description

20 BLISTER PACK in 1 BOX (50268-652-12) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-652-11)

Marketing

Marketing Status
Marketed Since 2021-01-07
Brand pilocarpine hydrochloride
Generic pilocarpine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47fb4499-fabd-6354-e063-6394a90a8c41", "openfda": {"unii": ["0WW6D218XJ"], "rxcui": ["1000913"], "spl_set_id": ["b85547d8-fcec-323d-e053-2995a90a4e7e"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 BOX (50268-652-12)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-652-11)", "package_ndc": "50268-652-12", "marketing_start_date": "20210107"}], "brand_name": "Pilocarpine Hydrochloride", "product_id": "50268-652_47fb4499-fabd-6354-e063-6394a90a8c41", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "50268-652", "generic_name": "Pilocarpine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pilocarpine Hydrochloride", "active_ingredients": [{"name": "PILOCARPINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077220", "marketing_category": "ANDA", "marketing_start_date": "20210107", "listing_expiration_date": "20271231"}