NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2113Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2113Add 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
71335-2113-17133521130120 TABLET in 1 BOTTLE (71335-2113-1)Marketed from Jan 31, 2025
71335-2113-27133521130230 TABLET in 1 BOTTLE (71335-2113-2)Marketed from Sep 7, 2022
71335-2113-37133521130350 TABLET in 1 BOTTLE (71335-2113-3)Marketed from Sep 7, 2022
71335-2113-47133521130414 TABLET in 1 BOTTLE (71335-2113-4)Marketed from Jan 31, 2025
71335-2113-57133521130540 TABLET in 1 BOTTLE (71335-2113-5)Marketed from Jan 31, 2025
71335-2113-67133521130660 TABLET in 1 BOTTLE (71335-2113-6)Marketed from Jan 31, 2025
71335-2113-77133521130728 TABLET in 1 BOTTLE (71335-2113-7)Marketed from Jan 31, 2025
71335-2113-87133521130810 TABLET in 1 BOTTLE (71335-2113-8)Marketed from Jan 31, 2025
71335-2113-9713352113096 TABLET in 1 BOTTLE (71335-2113-9)Marketed from Jan 31, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Doxycycline Hyclate
Generic name (nonproprietary)
doxycycline hyclate
Active ingredients
Doxycycline hyclate — 100 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207773
Marketing start
Listing expires
Other FDA classes
Tetracyclines (Chemical structure)
Identifiers
Product ID 71335-2113_2a8fc1ec-e0ab-4418-ac20-93d68fa4a5fcSPL ID 2a8fc1ec-e0ab-4418-ac20-93d68fa4a5fcSPL set ID 5b4390ed-a0ec-4ef8-864c-8a33a83653f9RxCUI 1650143UNII 19XTS3T51U
Pharmacologic class
Tetracycline-class Drug

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

N471335211301 followed by a unit qualifier and the quantity

Package 71335-2113-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 207773

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

FDA NDC Directory listings under ANDA 207773
ProductStrengthForm · routeLabelerProduct NDC
Doxycycline hyclateDoxycycline hyclate 100 mg/1TabletOralZydus Lifesciences Limited70771-1104
Doxycycline HyclateDoxycycline hyclate 100 mg/1TabletOralRedPharm Drug, Inc.67296-1431
Doxycycline HyclateDoxycycline hyclate 100 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8529
Doxycycline HyclateDoxycycline hyclate 100 mg/1TabletOralViona Pharmaceuticals Inc72578-001

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