Package 0172-6406-49

Brand: cromolyn sodium

Generic: cromolyn sodium
NDC Package

Package Facts

Identity

Package NDC 0172-6406-49
Digits Only 0172640649
Product NDC 0172-6406
Description

12 POUCH in 1 CARTON (0172-6406-49) / 5 VIAL, SINGLE-DOSE in 1 POUCH (0172-6406-05) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2000-01-18
Brand cromolyn sodium
Generic cromolyn sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRABRONCHIAL"], "spl_id": "38833b9a-b1dd-4e33-b8a3-806fa99eb4a4", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["831246"], "spl_set_id": ["8fe37a7a-edd6-4733-bb7e-e01c1906aeba"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CARTON (0172-6406-49)  / 5 VIAL, SINGLE-DOSE in 1 POUCH (0172-6406-05)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0172-6406-49", "marketing_start_date": "20000118"}], "brand_name": "Cromolyn Sodium", "product_id": "0172-6406_38833b9a-b1dd-4e33-b8a3-806fa99eb4a4", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "0172-6406", "generic_name": "Cromolyn Sodium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cromolyn Sodium", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "20 mg/2mL"}], "application_number": "ANDA075271", "marketing_category": "ANDA", "marketing_start_date": "20000118", "listing_expiration_date": "20261231"}