NDC codes

FDA NDC Directory
Product NDC (as listed)0480-3309Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00480-3309Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
0480-3309-0100480330901100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0480-3309-01)Marketed from Jan 27, 2023

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Theophylline
Generic name (nonproprietary)
theophylline
Active ingredients
Theophylline — 450 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Teva Pharmaceuticals, Inc.NDC labeler code 0480
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216961
Marketing start
Listing expires
Other FDA classes
Xanthines (Chemical structure)
Identifiers
Product ID 0480-3309_7d1746e6-4ce7-4a14-a2f8-c95bc8941b3cSPL ID 7d1746e6-4ce7-4a14-a2f8-c95bc8941b3cSPL set ID 25eabefa-518b-4030-9b72-01ac8b3deba9RxCUI 314241, 317769UNII C137DTR5RG
Pharmacologic class
Methylxanthine

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N400480330901 followed by a unit qualifier and the quantity

Package 00480-3309-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE Theophylline extended-release tablets are indicated for the treatment of the symptoms and reversible airflow obstruction associated with chronic asthma and other chronic lung diseases, e.g., emphysema and chronic bronchitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0480-3309

What is NDC 0480-3309?
0480-3309 is the product NDC for Theophylline, Theophylline 450 mg/1 tablet, extended release, listed with the FDA by Teva Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Theophylline.
What is the active ingredient?
Theophylline.
Who is the labeler?
Teva Pharmaceuticals, Inc., NDC labeler code 0480. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Theophylline?
40 other product NDCs are listed under this name. See all Theophylline NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Theophylline NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
TheophyllineTheophylline anhydrous 300 mg/1Tablet, Extended releaseOralAjanta Pharma USA Inc.27241-27227241-0272-01
TheophyllineTheophylline anhydrous 450 mg/1Tablet, Extended releaseOralAjanta Pharma USA Inc.27241-27327241-0273-01
TheophyllineTheophylline anhydrous 300 mg/1Tablet, Extended releaseOralStrides Pharma Science Limited64380-24364380-0243-01
TheophyllineTheophylline anhydrous 450 mg/1Tablet, Extended releaseOralStrides Pharma Science Limited64380-24464380-0244-01
TheophyllineTheophylline anhydrous 300 mg/1Tablet, Extended releaseOralPD-Rx Pharmaceuticals, Inc.72789-44172789-0441-01
TheophyllineTheophylline anhydrous 450 mg/1Tablet, Extended releaseOralPD-Rx Pharmaceuticals, Inc.72789-44272789-0442-01
TheophyllineTheophylline anhydrous 300 mg/1Tablet, Extended releaseOralHarman Finochem Limited82638-10582638-0105-02
TheophyllineTheophylline anhydrous 450 mg/1Tablet, Extended releaseOralHarman Finochem Limited82638-10682638-0106-02
TheophyllineTheophylline anhydrous 300 mg/1Tablet, Extended releaseOralZydus Lifesciences Limited70771-178270771-1782-01
TheophyllineTheophylline anhydrous 450 mg/1Tablet, Extended releaseOralZydus Lifesciences Limited70771-178370771-1783-01

All 41 Theophylline NDCs

Other NDCs under ANDA 216961

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 216961
ProductStrengthForm · routeLabelerProduct NDC
TheophyllineTheophylline 300 mg/1Tablet, Extended releaseOralTeva Pharmaceuticals, Inc.0480-3310

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