NDC codes

FDA NDC Directory
Product NDC (as listed)70710-1121Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70710-1121Add 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
70710-1121-170710112101100 TABLET, FILM COATED in 1 BOTTLE (70710-1121-1)Marketed from Jan 11, 2018

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209582
Marketing start
Listing expires
Other FDA classes
Tetracyclines (Chemical structure)
Identifiers
Product ID 70710-1121_24db9fe2-5c05-42d0-b113-307484699e9aSPL ID 24db9fe2-5c05-42d0-b113-307484699e9aSPL set ID bc321932-b600-4659-a499-1853991b4ab9RxCUI 1649429, 1650142, 1650444, 1652673UNII 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

N470710112101 followed by a unit qualifier and the quantity

Package 70710-1121-01. 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 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 g…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209582

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

FDA NDC Directory listings under ANDA 209582
ProductStrengthForm · routeLabelerProduct NDC
DoxycyclineDoxycycline 150 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1124
DoxycyclineDoxycycline 75 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1122
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1123
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2638
Doxycycline MonohydrateDoxycycline 100 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0319
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralProficient Rx LP82804-028
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-3809
DoxycyclineDoxycycline 75 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1007
DoxycyclineDoxycycline 50 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1006
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1008
DoxycyclineDoxycycline 150 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1009

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