theophylline
Generic: theophylline
Labeler: bionpharma inc.,Drug Facts
Product Profile
Brand Name
theophylline
Generic Name
theophylline
Labeler
bionpharma inc.,
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
theophylline anhydrous 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69452-267
Product ID
69452-267_07895277-4273-508f-e063-6394a90a40ea
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216300
Listing Expiration
2026-12-31
Marketing Start
2023-10-12
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69452267
Hyphenated Format
69452-267
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
theophylline (source: ndc)
Generic Name
theophylline (source: ndc)
Application Number
ANDA216300 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-267-20)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "07895277-4273-508f-e063-6394a90a40ea", "openfda": {"nui": ["N0000175790", "M0023046"], "unii": ["0I55128JYK"], "rxcui": ["317769"], "spl_set_id": ["63517422-45a0-4e78-8505-eca054068ee9"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Bionpharma Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-267-20)", "package_ndc": "69452-267-20", "marketing_start_date": "20231012"}], "brand_name": "Theophylline", "product_id": "69452-267_07895277-4273-508f-e063-6394a90a40ea", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "69452-267", "generic_name": "Theophylline", "labeler_name": "Bionpharma Inc.,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "300 mg/1"}], "application_number": "ANDA216300", "marketing_category": "ANDA", "marketing_start_date": "20231012", "listing_expiration_date": "20261231"}