Prescription drug · ANDA

Doxycycline Hyclate NDC 70518-4510

Doxycycline hyclate 100 mg/1 · Tablet, Film coated · Oral · REMEDYREPACK INC.

NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4510Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4510Add 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
70518-4510-07051845100014 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4510-0)Marketed from Oct 24, 2025

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 Hyclate
Generic name (nonproprietary)
doxycycline hyclate
Active ingredients
Doxycycline hyclate — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 062269
Marketing start
Listing expires
Other FDA classes
Tetracyclines (Chemical structure)
Identifiers
Product ID 70518-4510_5b86d02d-fb8b-b5a0-e063-6394a90ab78fSPL ID 5b86d02d-fb8b-b5a0-e063-6394a90ab78f
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

N470518451000 followed by a unit qualifier and the quantity

Package 70518-4510-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 062269

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

FDA NDC Directory listings under ANDA 062269
ProductStrengthForm · routeLabelerProduct NDC
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3214
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralRedpharm Drug67296-2189
Doxycycline HyclateDoxycycline hyclate 50 mg/1Tablet, Film coatedOralJG Pharma Inc.72143-262
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralPURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS24658-310
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4836
Targadoxdoxycycline hyclateDoxycycline hyclate 50 mg/1TabletOralJourney Medical Corporation69489-111
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralHealth Department, Oklahoma State83112-100
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7800
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7546
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7547
Doxycycline HyclateDoxycycline hyclate 100 mg/1Tablet, Film coatedOralEpic Pharma, LLC42806-310

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Doxycycline Hyclate NDC 70518-4510 | Med-Code