NDC codes

FDA NDC Directory
Product NDC (as listed)60687-344Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0344Add 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
60687-344-25606870344256068703442530 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-344-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-344-95)Marketed from Dec 5, 2017

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
Generic name (nonproprietary)
doxycycline
Active ingredients
Doxycycline — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 065285
Marketing start
Listing expires
Other FDA classes
Tetracyclines (Chemical structure)
Identifiers
Product ID 60687-344_2abe1780-d1e3-a90a-e063-6294a90a64eeSPL ID 2abe1780-d1e3-a90a-e063-6294a90a64eeSPL set ID adc6ba78-8dd7-47af-a7b4-c2215557696bRxCUI 1650142UNII N12000U13O
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

N460687034425 followed by a unit qualifier and the quantity

Package 60687-0344-25. 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 the effectiveness of doxycycline tablets, USP and other antibacterial drugs, doxycycline tablets, USP 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. Doxycycline Tablets, USP are indicated for the treatment of the following infections: Rocky Mountain spotted fever, typhu…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-344

What is NDC 60687-344?
60687-344 is the product NDC for Doxycycline, Doxycycline 100 mg/1 tablet, film coated, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Doxycycline.
What is the active ingredient?
Doxycycline.
Who is the labeler?
American Health Packaging, NDC labeler code 60687. 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?
136 other product NDCs are listed under this name. See all Doxycycline 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 NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DoxycyclineDoxycycline 100 mg/1CapsuleOralREMEDYREPACK INC.70518-476270518-4762-00
doxycyclineDoxycycline 50 mg/1CapsuleOralSafecor Health, LLC48433-15848433-0158-03
doxycyclineDoxycycline 100 mg/1CapsuleOralSafecor Health, LLC48433-15948433-0159-03
doxycyclineDoxycycline 100 mg/1CapsuleOralCoupler LLC67046-126067046-1260-03
doxycyclineDoxycycline hyclate 100 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-417668788-4176-0068788-4176-0168788-4176-02+3 more
doxycyclineDoxycycline hyclate 100 mg/1CapsuleOralREMEDYREPACK INC.70518-465570518-4655-0070518-4655-01
DoxycyclineDoxycycline hyclate 100 mg/100mgInjection, Powder, Lyophilized, For solutionIntravenousSteriscience Specialties Private Limited82449-00882449-0008-02
DoxycyclineDoxycycline 100 mg/1CapsuleOralAmerican Health Packaging60687-94360687-0943-21
DoxycyclineDoxycycline hyclate 100 mg/10mLInjection, Powder, Lyophilized, For solutionIntravenousJVET PHARMACEUTICALS LLC86211-11686211-0116-10
DoxycyclineDoxycycline 40 mg/1CapsuleOralAiPing Pharmaceutical, Inc.11788-13411788-0134-30

All 137 Doxycycline NDCs

Other NDCs under ANDA 065285

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

FDA NDC Directory listings under ANDA 065285
ProductStrengthForm · routeLabelerProduct NDC
DoxycyclineDoxycycline 50 mg/1Tablet, Film coatedOralLannett Company, Inc.0527-1335
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralLannett Company, Inc.0527-1338
DoxycyclineDoxycycline 75 mg/1Tablet, Film coatedOralLannett Company, Inc.0527-1535
DoxycyclineDoxycycline 150 mg/1Tablet, Film coatedOralLannett Company, Inc.0527-1537
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-9410

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