Package 16571-600-96

Brand: cromolyn sodium

Generic: cromolyn sodium
NDC Package

Package Facts

Identity

Package NDC 16571-600-96
Digits Only 1657160096
Product NDC 16571-600
Description

12 POUCH in 1 CARTON (16571-600-96) / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2011-12-05
Brand cromolyn sodium
Generic cromolyn sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ca2c72ae-db00-4694-9fd0-d4b6b45f8108", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["831261"], "spl_set_id": ["61c9cb85-129e-4490-b5f7-357307fcecbf"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CARTON (16571-600-96)  / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE", "package_ndc": "16571-600-96", "marketing_start_date": "20111205"}], "brand_name": "CROMOLYN SODIUM", "product_id": "16571-600_ca2c72ae-db00-4694-9fd0-d4b6b45f8108", "dosage_form": "SOLUTION, CONCENTRATE", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "16571-600", "generic_name": "CROMOLYN SODIUM", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CROMOLYN SODIUM", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "100 mg/5mL"}], "application_number": "ANDA202583", "marketing_category": "ANDA", "marketing_start_date": "20111205", "listing_expiration_date": "20261231"}