Package 71321-500-10

Brand: theophylline

Generic: theophylline
NDC Package

Package Facts

Identity

Package NDC 71321-500-10
Digits Only 7132150010
Product NDC 71321-500
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71321-500-10)

Marketing

Marketing Status
Marketed Since 2025-09-30
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": "9c1ede62-fd47-41f4-96da-93d65133042d", "openfda": {"nui": ["N0000175790", "M0023046"], "unii": ["0I55128JYK"], "rxcui": ["237178", "317769", "346574"], "spl_set_id": ["7b98b47d-0a6e-4621-b047-bdb8bcef4836"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Brandywine Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71321-500-10)", "package_ndc": "71321-500-10", "marketing_start_date": "20250930"}], "brand_name": "Theophylline", "product_id": "71321-500_9c1ede62-fd47-41f4-96da-93d65133042d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "71321-500", "generic_name": "Theophylline", "labeler_name": "Brandywine Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "100 mg/1"}], "application_number": "ANDA087400", "marketing_category": "ANDA", "marketing_start_date": "20250930", "listing_expiration_date": "20261231"}