NDC codes

FDA NDC Directory
Product NDC (as listed)23155-136Labeler and product segments. Claims need a package NDC.
Product NDC at billing width23155-0136Add 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
23155-136-032315501360330 TABLET in 1 BOTTLE (23155-136-03)Marketed from May 1, 2012
23155-136-0523155013605500 TABLET in 1 BOTTLE (23155-136-05)Marketed from May 1, 2012
23155-136-112315501361110 TABLET in 1 BLISTER PACK (23155-136-11)Marketed from May 1, 2012
23155-136-302315501363030 TABLET in 1 CARTON (23155-136-30)Marketed from May 1, 2012

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 — 150 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091605
Marketing start
Listing expires
Other FDA classes
Tetracyclines (Chemical structure)
Identifiers
Product ID 23155-136_ec6854e5-3f41-4b8f-be77-49e3bd19f7c4SPL ID ec6854e5-3f41-4b8f-be77-49e3bd19f7c4SPL set ID 2bcde264-5f6f-47f6-ae2e-1b7010deacf7RxCUI 1649429, 1650142, 1650444, 1652673UNII N12000U13OUPC 0323155135053
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

N423155013603 followed by a unit qualifier and the quantity

Package 23155-0136-03. 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 tablets and other antibacterial drugs, doxycycline tablets 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 is indicated for the treatment of the following infections: Rocky mountain spotted fever, typhus fever and the typhus group…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 091605

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

FDA NDC Directory listings under ANDA 091605
ProductStrengthForm · routeLabelerProduct NDC
DoxycyclineDoxycycline 50 mg/1TabletOralChartwell RX, LLC62135-725
DoxycyclineDoxycycline 100 mg/1TabletOralChartwell RX, LLC62135-726
DoxycyclineDoxycycline 100 mg/1TabletOralProficient Rx LP82804-264
DoxycyclineDoxycycline 100 mg/1TabletOralNorthwind Health Company, LLC51655-350
DoxycyclineDoxycycline 100 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-135
DoxycyclineDoxycycline 50 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-133
DoxycyclineDoxycycline 75 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-134
DoxycyclineDoxycycline 100 mg/1TabletOralA-S Medication Solutions50090-1462

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