NDC codes

FDA NDC Directory
Product NDC (as listed)69842-686Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69842-0686Add 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
69842-686-07698420686071 BLISTER PACK in 1 CARTON (69842-686-07) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACKMarketed from Jan 31, 2017
69842-686-30698420686303 BLISTER PACK in 1 CARTON (69842-686-30) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACKMarketed from Jan 31, 2017
69842-686-60698420686606 BLISTER PACK in 1 CARTON (69842-686-60) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACKMarketed from Jan 31, 2017

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Loratadine
Generic name (nonproprietary)
loratadine
Active ingredients
Loratadine — 10 mg/1
Dosage form
Capsule, Liquid filled
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206214
Marketing start
Listing expires
Identifiers
Product ID 69842-686_4deaf048-b4b9-546e-e063-6394a90a4fdbSPL ID 4deaf048-b4b9-546e-e063-6394a90a4fdbSPL set ID 899800a7-89bc-4a39-88b0-f19d78934dafRxCUI 828269UNII 7AJO3BO7QN

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

N469842068607 followed by a unit qualifier and the quantity

Package 69842-0686-07. 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)

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 206214

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

FDA NDC Directory listings under ANDA 206214
ProductStrengthForm · routeLabelerProduct NDC
LoratadineLoratadine 10 mg/1Capsule, Liquid filledOralMARKSANS PHARMA LIMITED25000-021
Allergy ReliefloratadineLoratadine 10 mg/1Capsule, Liquid filledOralTARGET CORPORATION11673-986
LoratadineLoratadine 10 mg/1Capsule, Liquid filledOralSMART SENSE (KMART)49738-686
Allergy ReliefloratadineLoratadine 10 mg/1Capsule, Liquid filledOralCHAIN DRUG MARKETING ASSOCIATION, INC.83324-103
Allergy ReliefloratadineLoratadine 10 mg/1Capsule, Liquid filledOralSafeway21130-195
LoratadineLoratadine 10 mg/1Capsule, Liquid filledOralKROGER COMPANY41226-686
Allergy ReliefloratadineLoratadine 10 mg/1Capsule, Liquid filledOralCARDINAL HEALTH 110, LLC. DBA LEADER70000-0755
LoratadineLoratadine 10 mg/1Capsule, Liquid filledOralTIME CAP LABORATORIES INC49483-686
Wal-ItinloratadineLoratadine 10 mg/1Capsule, Liquid filledOralWALGREENS0363-1686

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