Doxycycline NDC 0527-1535

NDC codes

FDA NDC Directory

Product NDC (as listed)0527-1535Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00527-1535Add 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 NDC	11-digit (billing)	Package	Copy
0527-1535-01	00527153501	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1535-01)Marketed from Aug 25, 2008

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 — 75 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Lannett Company, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 065285
Marketing start: Aug 25, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Tetracyclines (Chemical structure)
Identifiers: Product ID 0527-1535_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

N400527153501 followed by a unit qualifier and the quantity

Package 00527-1535-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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
Product	Strength	Form · route	Labeler	Product NDC
Doxycycline	Doxycycline 150 mg/1	Tablet, Film coatedOral	Lannett Company, Inc.	0527-1537
Doxycycline	Doxycycline 50 mg/1	Tablet, Film coatedOral	Lannett Company, Inc.	0527-1335
Doxycycline	Doxycycline 100 mg/1	Tablet, Film coatedOral	Lannett Company, Inc.	0527-1338
Doxycycline	Doxycycline 100 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-344
Doxycycline	Doxycycline 100 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-9410