Package 0713-0135-10

Brand: prochlorperazine

Generic: prochlorperazine
NDC Package

Package Facts

Identity

Package NDC 0713-0135-10
Digits Only 0713013510
Product NDC 0713-0135
Description

1000 BLISTER PACK in 1 CARTON (0713-0135-10) / 1 SUPPOSITORY in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 1993-11-30
Brand prochlorperazine
Generic prochlorperazine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "462a6c34-db6d-8d31-e063-6294a90ae196", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["YHP6YLT61T"], "rxcui": ["198159"], "spl_set_id": ["9595346e-76e5-e155-341b-ffaaafb885ab"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Cosette Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 BLISTER PACK in 1 CARTON (0713-0135-10)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "0713-0135-10", "marketing_start_date": "19931130"}, {"sample": false, "description": "12 BLISTER PACK in 1 CARTON (0713-0135-12)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "0713-0135-12", "marketing_start_date": "19931130"}], "brand_name": "Prochlorperazine", "product_id": "0713-0135_462a6c34-db6d-8d31-e063-6294a90ae196", "dosage_form": "SUPPOSITORY", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0713-0135", "generic_name": "Prochlorperazine", "labeler_name": "Cosette Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine", "active_ingredients": [{"name": "PROCHLORPERAZINE", "strength": "25 mg/1"}], "application_number": "ANDA040058", "marketing_category": "ANDA", "marketing_start_date": "19931130", "listing_expiration_date": "20261231"}