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Last Updated: March 19, 2026

Details for New Drug Application (NDA): 087400

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NDA 087400 describes THEOPHYLLINE, which is a drug marketed by Cent Pharms, Hospira, Inwood Labs, Sandoz, Kv Pharm, Scherer Rp, Alpharma Us Pharms, Cenci, Chartwell Rx, Halsey, Pharm Assoc, Precision Dose, Roxane, Sun Pharma Canada, Wockhardt, Chartwell Molecular, Tris Pharma Inc, Able, Ajanta Pharma Ltd, Alembic, Amneal, Annora Pharma, Bionpharma, Glenmark Pharms Ltd, Harman Finochem, Heritage Pharma Avet, Mpp Pharma, Nostrum Pharms Llc, Rhodes Pharms, Strides Pharma, Teva Pharms Inc, Velzen Pharma Pvt, Zydus Lifesciences, B Braun, Baxter Hlthcare, and Hospira Inc, and is included in fifty-five NDAs. It is available from twenty-seven suppliers. Additional details are available on the THEOPHYLLINE profile page.

The generic ingredient in THEOPHYLLINE is theophylline. There are thirty-six drug master file entries for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the theophylline profile page.

Summary for 087400

Tradename:	THEOPHYLLINE
Applicant:	Nostrum Pharms Llc
Ingredient:	theophylline
Patents:	0

Pharmacology for NDA: 087400

Medical Subject Heading (MeSH) Categories for 087400

Bronchodilator Agents
Phosphodiesterase Inhibitors
Purinergic P1 Receptor Antagonists
Vasodilator Agents

Suppliers and Packaging for NDA: 087400

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
THEOPHYLLINE	theophylline	TABLET, EXTENDED RELEASE;ORAL	087400	ANDA	Brandywine Pharmaceuticals, LLC	71321-500	71321-500-10	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71321-500-10)
THEOPHYLLINE	theophylline	TABLET, EXTENDED RELEASE;ORAL	087400	ANDA	Brandywine Pharmaceuticals, LLC	71321-501	71321-501-10	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71321-501-10)

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET, EXTENDED RELEASE;ORAL			Strength	300MG
Approval Date:	Jan 11, 1983	TE:	AB	RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET, EXTENDED RELEASE;ORAL			Strength	100MG
Approval Date:	Feb 21, 1985	TE:		RLD:	No

Profile for product number 004

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET, EXTENDED RELEASE;ORAL			Strength	200MG
Approval Date:	Feb 21, 1985	TE:		RLD:	No

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