Package 0121-4820-40

Brand: theophylline

Generic: theophylline
NDC Package

Package Facts

Identity

Package NDC 0121-4820-40
Digits Only 0121482040
Product NDC 0121-4820
Description

4 TRAY in 1 CASE (0121-4820-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4820-15)

Marketing

Marketing Status
Marketed Since 2016-12-16
Brand theophylline
Generic theophylline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "895f63e5-665b-4227-8e44-6971ba5ce294", "openfda": {"unii": ["C137DTR5RG"], "rxcui": ["313306"], "spl_set_id": ["32b9780f-c46f-4e0f-9641-2cab60600e6e"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 TRAY in 1 CASE (0121-4820-40)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4820-15)", "package_ndc": "0121-4820-40", "marketing_start_date": "20161216"}], "brand_name": "THEOPHYLLINE", "product_id": "0121-4820_895f63e5-665b-4227-8e44-6971ba5ce294", "dosage_form": "SOLUTION", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "0121-4820", "generic_name": "THEOPHYLLINE", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "THEOPHYLLINE", "active_ingredients": [{"name": "THEOPHYLLINE", "strength": "80 mg/15mL"}], "application_number": "ANDA206344", "marketing_category": "ANDA", "marketing_start_date": "20161216", "listing_expiration_date": "20261231"}