What is NDC 70710-1124?

70710-1124 is the product NDC for Doxycycline, Doxycycline 150 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Zydus Pharmaceuticals USA Inc., NDC labeler code 70710. 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?

136 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Doxycycline NDC 70710-1124 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70710-1124Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70710-1124Add 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
70710-1124-1	7071011240170710112401	100 TABLET, FILM COATED in 1 BOTTLE (70710-1124-1)Marketed from Jan 11, 2018
70710-1124-3	7071011240370710112403	30 TABLET, FILM COATED in 1 BOTTLE (70710-1124-3)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 — 150 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Zydus Pharmaceuticals USA Inc.NDC labeler code 70710
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209582
Marketing start: Jan 11, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Tetracyclines (Chemical structure)
Identifiers: Product ID 70710-1124_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

N470710112401 followed by a unit qualifier and the quantity

Package 70710-1124-01. 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 Apr 10, 2025.

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)

About NDC 70710-1124

What is NDC 70710-1124?: 70710-1124 is the product NDC for Doxycycline, Doxycycline 150 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 2 package NDCs, 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?: Zydus Pharmaceuticals USA Inc., NDC labeler code 70710. 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?: 136 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Doxycycline	Doxycycline 100 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4762	70518-4762-00
doxycycline	Doxycycline 50 mg/1	CapsuleOral	Safecor Health, LLC	48433-158	48433-0158-03
doxycycline	Doxycycline 100 mg/1	CapsuleOral	Safecor Health, LLC	48433-159	48433-0159-03
doxycycline	Doxycycline 100 mg/1	CapsuleOral	Coupler LLC	67046-1260	67046-1260-03
doxycycline	Doxycycline hyclate 100 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-4176	68788-4176-0068788-4176-0168788-4176-02+3 more
doxycycline	Doxycycline hyclate 100 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4655	70518-4655-0070518-4655-01
Doxycycline	Doxycycline hyclate 100 mg/100mg	Injection, Powder, Lyophilized, For solutionIntravenous	Steriscience Specialties Private Limited	82449-008	82449-0008-02
Doxycycline	Doxycycline 100 mg/1	CapsuleOral	American Health Packaging	60687-943	60687-0943-21
Doxycycline	Doxycycline hyclate 100 mg/10mL	Injection, Powder, Lyophilized, For solutionIntravenous	JVET PHARMACEUTICALS LLC	86211-116	86211-0116-10
Doxycycline	Doxycycline 40 mg/1	CapsuleOral	AiPing Pharmaceutical, Inc.	11788-134	11788-0134-30

All 137 Doxycycline NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Doxycycline	Doxycycline 50 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1006
Doxycycline	Doxycycline 75 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1007
Doxycycline	Doxycycline 100 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1008
Doxycycline	Doxycycline 150 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1009
Doxycycline	Doxycycline 100 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1123
Doxycycline	Doxycycline 50 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1121
Doxycycline	Doxycycline 75 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1122
Doxycycline	Doxycycline 100 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2638
Doxycycline	Doxycycline 100 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-3809
Doxycycline Monohydrate	Doxycycline 100 mg/1	Tablet, Film coatedOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0319
Doxycycline	Doxycycline 100 mg/1	Tablet, Film coatedOral	Proficient Rx LP	82804-028