Package 61314-237-10

Brand: cromolyn sodium

Generic: cromolyn sodium
NDC Package

Package Facts

Identity

Package NDC 61314-237-10
Digits Only 6131423710
Product NDC 61314-237
Product ID 61314-237_4d6f900a-fa36-445e-80d5-54c8cc5baf34
Description

10 mL in 1 BOTTLE, PLASTIC (61314-237-10)

Marketing

Marketing Status
Marketed Since 1999-06-29
Brand cromolyn sodium
Generic cromolyn sodium
Sample Package No

Linked Drug Pages (1)

Cromolyn Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "4d6f900a-fa36-445e-80d5-54c8cc5baf34", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["831109"], "spl_set_id": ["b32851c3-cd97-4be4-a09c-1deab1d6966b"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOTTLE, PLASTIC (61314-237-10)", "package_ndc": "61314-237-10", "marketing_start_date": "19990629"}], "brand_name": "Cromolyn Sodium", "product_id": "61314-237_4d6f900a-fa36-445e-80d5-54c8cc5baf34", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "61314-237", "generic_name": "Cromolyn Sodium", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cromolyn Sodium", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "40 mg/mL"}], "application_number": "ANDA075282", "marketing_category": "ANDA", "marketing_start_date": "19990629", "listing_expiration_date": "20261231"}