Package 43063-695-20

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 43063-695-20
Digits Only 4306369520
Product NDC 43063-695
Description

20 TABLET in 1 BOTTLE, PLASTIC (43063-695-20)

Marketing

Marketing Status
Marketed Since 2017-02-21
Brand famotidine
Generic famotidine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41478927-2719-0a32-e063-6294a90acdc9", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0343063695906"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["66f0bf15-ff35-426a-b40c-0d0da79d0861"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (43063-695-20)", "package_ndc": "43063-695-20", "marketing_start_date": "20170221"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-695-30)", "package_ndc": "43063-695-30", "marketing_start_date": "20160726"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-695-60)", "package_ndc": "43063-695-60", "marketing_start_date": "20160726"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-695-90)", "package_ndc": "43063-695-90", "marketing_start_date": "20160726"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (43063-695-93)", "package_ndc": "43063-695-93", "marketing_start_date": "20160726"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (43063-695-95)", "package_ndc": "43063-695-95", "marketing_start_date": "20210222"}], "brand_name": "Famotidine", "product_id": "43063-695_41478927-2719-0a32-e063-6294a90acdc9", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "43063-695", "generic_name": "Famotidine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA075805", "marketing_category": "ANDA", "marketing_start_date": "20010416", "listing_expiration_date": "20261231"}