NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1006Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1006Add 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
70771-1006-17077110060170771100601100 TABLET, FILM COATED in 1 BOTTLE (70771-1006-1)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
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
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 70771-1006_9139fc59-1c7a-446d-92ed-2581324664fcSPL ID 9139fc59-1c7a-446d-92ed-2581324664fc
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

N470771100601 followed by a unit qualifier and the quantity

Package 70771-1006-01. 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

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

About NDC 70771-1006

What is NDC 70771-1006?
70771-1006 is the product NDC for Doxycycline, Doxycycline 50 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, 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 Lifesciences Limited, NDC labeler code 70771. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DoxycyclineDoxycycline 100 mg/1CapsuleOralREMEDYREPACK INC.70518-476270518-4762-00
doxycyclineDoxycycline 50 mg/1CapsuleOralSafecor Health, LLC48433-15848433-0158-03
doxycyclineDoxycycline 100 mg/1CapsuleOralSafecor Health, LLC48433-15948433-0159-03
doxycyclineDoxycycline 100 mg/1CapsuleOralCoupler LLC67046-126067046-1260-03
doxycyclineDoxycycline hyclate 100 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-417668788-4176-0068788-4176-0168788-4176-02+3 more
doxycyclineDoxycycline hyclate 100 mg/1CapsuleOralREMEDYREPACK INC.70518-465570518-4655-0070518-4655-01
DoxycyclineDoxycycline hyclate 100 mg/100mgInjection, Powder, Lyophilized, For solutionIntravenousSteriscience Specialties Private Limited82449-00882449-0008-02
DoxycyclineDoxycycline 100 mg/1CapsuleOralAmerican Health Packaging60687-94360687-0943-21
DoxycyclineDoxycycline hyclate 100 mg/10mLInjection, Powder, Lyophilized, For solutionIntravenousJVET PHARMACEUTICALS LLC86211-11686211-0116-10
DoxycyclineDoxycycline 40 mg/1CapsuleOralAiPing Pharmaceutical, Inc.11788-13411788-0134-30

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
ProductStrengthForm · routeLabelerProduct NDC
DoxycyclineDoxycycline 75 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1007
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1008
DoxycyclineDoxycycline 150 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1009
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1123
DoxycyclineDoxycycline 50 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1121
DoxycyclineDoxycycline 75 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1122
DoxycyclineDoxycycline 150 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-1124
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2638
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-3809
Doxycycline MonohydrateDoxycycline 100 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0319
DoxycyclineDoxycycline 100 mg/1Tablet, Film coatedOralProficient Rx LP82804-028

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