Package 71205-230-10

Brand: cromolyn sodium

Generic: cromolyn sodium
NDC Package

Package Facts

Identity

Package NDC 71205-230-10
Digits Only 7120523010
Product NDC 71205-230
Description

10 mL in 1 BOTTLE, PLASTIC (71205-230-10)

Marketing

Marketing Status
Marketed Since 2019-03-01
Brand cromolyn sodium
Generic cromolyn sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "1c80e622-005d-44f1-a5a9-2e0acd59e485", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["831109"], "spl_set_id": ["34ef00e8-0c01-4225-9a40-822ab245752a"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOTTLE, PLASTIC (71205-230-10)", "package_ndc": "71205-230-10", "marketing_start_date": "20190301"}], "brand_name": "Cromolyn Sodium", "product_id": "71205-230_1c80e622-005d-44f1-a5a9-2e0acd59e485", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "71205-230", "generic_name": "Cromolyn Sodium", "labeler_name": "Proficient Rx LP", "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"}