NDC codes

FDA NDC Directory
Product NDC (as listed)0527-1335Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00527-1335Add 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
0527-1335-0100527133501100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1335-01)Marketed from Dec 8, 2005

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)
Doxycycline
Generic name (nonproprietary)
doxycycline
Active ingredients
Doxycycline — 50 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Lannett Company, Inc.NDC labeler code 0527
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 0527-1335_dc960a6c-1b09-4049-a1e9-0109576b1d30SPL ID dc960a6c-1b09-4049-a1e9-0109576b1d30SPL set ID 4999bbd9-44ed-4749-9730-be2337bdf490RxCUI 1649429, 1650142, 1650444, 1652673UNII N12000U13OUPC 0305271537300, 0305271535016
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

N400527133501 followed by a unit qualifier and the quantity

Package 00527-1335-01. 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 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 0527-1335

What is NDC 0527-1335?
0527-1335 is the product NDC for Doxycycline, Doxycycline 50 mg/1 tablet, film coated, listed with the FDA by Lannett Company, Inc.. 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?
Lannett Company, Inc., NDC labeler code 0527. 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?
135 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 136 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 100 mg/1Tablet, Film coatedOralLannett Company, Inc.0527-1338
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-344
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-9410
DoxycyclineDoxycycline 75 mg/1Tablet, Film coatedOralLannett Company, Inc.0527-1535
DoxycyclineDoxycycline 150 mg/1Tablet, Film coatedOralLannett Company, Inc.0527-1537

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