NDC codes

FDA NDC Directory
Product NDC (as listed)72789-276Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0276Add 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
72789-276-017278902760172789027601100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-01)Marketed from Jan 19, 2024
72789-276-0772789027607727890276077 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-07)Marketed from Jan 19, 2024
72789-276-10727890276107278902761010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-10)Marketed from Jul 13, 2023
72789-276-14727890276147278902761414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-14)Marketed from Nov 18, 2022
72789-276-20727890276207278902762020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-20)Marketed from Nov 17, 2022
72789-276-28727890276287278902762828 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-28)Marketed from Aug 20, 2025
72789-276-717278902767172789027671210 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-71)Marketed from Jan 17, 2023
72789-276-747278902767472789027674400 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-74)Marketed from Jan 17, 2023
72789-276-827278902768272789027682500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-82)Marketed from Oct 7, 2022
72789-276-857278902768572789027685330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-85)Marketed from Feb 20, 2024
72789-276-877278902768772789027687300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-87)Marketed from Mar 2, 2023
72789-276-90727890276907278902769090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-90)Marketed from Jan 17, 2023
72789-276-937278902769372789027693180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-93)Marketed from Jan 17, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Doxycycline Hyclate
Generic name (nonproprietary)
doxycycline hyclate
Active ingredients
Doxycycline hyclate — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 72789
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 062677
Marketing start
Listing expires
Other FDA classes
Tetracyclines (Chemical structure)
Identifiers
Product ID 72789-276_56d253f7-dcc7-f5e9-e063-6294a90a92cbSPL ID 56d253f7-dcc7-f5e9-e063-6294a90a92cbSPL set ID 1401d590-0967-4c6b-b52b-a83e9f6df097RxCUI 1650143UNII 19XTS3T51UUPC 0372789276717
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

N472789027601 followed by a unit qualifier and the quantity

Package 72789-0276-01. 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 To reduce the development of drug-resistant bacteria and maintain effectiveness of doxycycline hyclate and other antibacterial drugs, doxycycline hyclate should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Treatment: Doxycycline is indicated for the treatment of the following infections: Rocky Mountain spotted fever, typhus fever and the t…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72789-276

What is NDC 72789-276?
72789-276 is the product NDC for Doxycycline Hyclate, Doxycycline hyclate 100 mg/1 tablet, film coated, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 13 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Doxycycline Hyclate.
What is the active ingredient?
Doxycycline hyclate.
Who is the labeler?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Doxycycline Hyclate?
175 other product NDCs are listed under this name. See all Doxycycline Hyclate 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 Doxycycline Hyclate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Doxycycline HyclateDoxycycline hyclate 100 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-02987441-0029-01
Doxycycline HyclateDoxycycline hyclate 100 mg/1CapsuleOralCoupler LLC67046-013567046-0135-03
Doxycycline HyclateDoxycycline hyclate 50 mg/1TabletOralStrides Pharma Science Limited64380-22564380-0225-01
Doxycycline HyclateDoxycycline hyclate 100 mg/1TabletOralStrides Pharma Science Limited64380-22664380-0226-02
Doxycycline HyclateDoxycycline hyclate 100 mg/1CapsuleOralREMEDYREPACK INC.70518-465870518-4658-00
Doxycycline HyclateDoxycycline hyclate 50 mg/1CapsuleOralZhejiang Yongtai Pharmaceutical Co., Ltd69434-01669434-0016-0369434-0016-06
Doxycycline HyclateDoxycycline hyclate 100 mg/1CapsuleOralZhejiang Yongtai Pharmaceutical Co., Ltd69434-01769434-0017-0369434-0017-06
Doxycycline HyclateDoxycycline hyclate 100 mg/1TabletOralREMEDYREPACK INC.70518-454470518-4544-00
Doxycycline HyclateDoxycycline hyclate 100 mg/1CapsuleOralMacleods Pharmaceuticals Limited33342-38633342-0386-0833342-0386-1233342-0386-15
Doxycycline HyclateDoxycycline hyclate 100 mg/1TabletOralMacleods Pharmaceuticals Limited33342-39233342-0392-0533342-0392-0833342-0392-11+2 more

All 176 Doxycycline Hyclate NDCs

Other NDCs under ANDA 062677

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

FDA NDC Directory listings under ANDA 062677
ProductStrengthForm · routeLabelerProduct NDC
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralAvPAK50268-279
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralSun Pharmaceutical Industries, Inc.53489-120
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3213
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-319
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-419

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