NDC codes

FDA NDC Directory
Product NDC (as listed)68999-626Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68999-0626Add 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
68999-626-02689990626026899906260220 TABLET, FILM COATED in 1 BOTTLE (68999-626-02)Marketed from Jun 24, 2022
68999-626-056899906260568999062605500 TABLET, FILM COATED in 1 BOTTLE (68999-626-05)Marketed from Sep 17, 2025
68999-626-066899906260668999062606100 TABLET, FILM COATED in 1 BOTTLE (68999-626-06)Marketed from Jun 24, 2022
68999-626-1068999062610689990626101000 TABLET, FILM COATED in 1 BOTTLE (68999-626-10)Marketed from Sep 1, 2021
68999-626-126899906261268999062612120 TABLET, FILM COATED in 1 BOTTLE (68999-626-12)Marketed from Sep 17, 2025
68999-626-236899906262368999062623210 TABLET, FILM COATED in 1 BOTTLE (68999-626-23)Marketed from Sep 1, 2021
68999-626-28689990626286899906262828 TABLET, FILM COATED in 1 BOTTLE (68999-626-28)Marketed from Sep 1, 2021
68999-626-30689990626306899906263030 TABLET, FILM COATED in 1 BOTTLE (68999-626-30)Marketed from Nov 12, 2021
68999-626-316899906263168999062631300 TABLET, FILM COATED in 1 BOTTLE (68999-626-31)Marketed from Sep 1, 2021
68999-626-406899906264068999062640400 TABLET, FILM COATED in 1 BOTTLE (68999-626-40)Marketed from Sep 1, 2021
68999-626-50689990626506899906265050 TABLET, FILM COATED in 1 BOTTLE (68999-626-50)Marketed from Sep 1, 2021
68999-626-9668999062696689990626962000 TABLET, FILM COATED in 1 BOTTLE (68999-626-96)Marketed from Sep 17, 2025

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
Chartwell Governmental & Specialty RX, LLCNDC labeler code 68999
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 062505
Marketing start
Listing expires
Other FDA classes
Tetracyclines (Chemical structure)
Identifiers
Product ID 68999-626_40076faf-09c3-f4ab-e063-6394a90ab3c1SPL ID 40076faf-09c3-f4ab-e063-6394a90ab3c1SPL set ID b8486639-7eb9-4610-9cd4-0e922045d592RxCUI 1649405, 1649988, 1650030, 1650143, 1652674UNII N12000U13O, 19XTS3T51UUPC 0368999626404, 0368999626282, 0368999625605, 0368999985501, 0368999984504, 0368999417460, 0368999626305, 0368999626060, 0368999626312, 0368999626503
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

N468999062602 followed by a unit qualifier and the quantity

Package 68999-0626-02. 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 and other antibacterial drugs, doxycycline 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 typhus group, Q fev…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68999-626

What is NDC 68999-626?
68999-626 is the product NDC for Doxycycline Hyclate, Doxycycline hyclate 100 mg/1 tablet, film coated, listed with the FDA by Chartwell Governmental & Specialty RX, LLC. It has 12 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?
Chartwell Governmental & Specialty RX, LLC, NDC labeler code 68999. 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 062505

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

FDA NDC Directory listings under ANDA 062505
ProductStrengthForm · routeLabelerProduct NDC
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4981
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-298
Doxycycline HyclateDoxycycline hyclate 50 mg/1Tablet, Film coatedOralChartwell RX LLC62135-625
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralChartwell RX LLC62135-626
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralRedpharm Drug, Inc.67296-1456
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5265
Doxycycline HyclateDoxycycline hyclate 50 mg/1Tablet, Film coatedOralChartwell Governmental & Specialty RX, LLC68999-625
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralProficient Rx LP71205-697
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1686
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOraldirect rx72189-127

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