NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4699Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4699Add 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
70518-4699-0705184699007051846990030 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4699-0)Marketed from Jul 15, 2026

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)
Quetiapine
Generic name (nonproprietary)
quetiapine
Active ingredients
Quetiapine fumarate — 200 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204253
Marketing start
Listing expires
Identifiers
Product ID 70518-4699_56a68e80-b365-6b1b-e063-6294a90ab589SPL ID 56a68e80-b365-6b1b-e063-6294a90ab589SPL set ID 67872105-4ec6-4d46-b3b4-c672c93576d2RxCUI 721791UNII 2S3PL1B6UJ
Pharmacologic class
Atypical Antipsychotic

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

N470518469900 followed by a unit qualifier and the quantity

Package 70518-4699-00. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Quetiapine extended-release tablets are an atypical antipsychotic indicated for the treatment of: • Schizophrenia ( 1.1 ) • Bipolar I disorder, manic, or mixed episodes ( 1.2 ) • Bipolar disorder, depressive episodes ( 1.2 ) • Major depressive disorder, adjunctive therapy with antidepressants ( 1.3 ) 1.1 Schizophrenia Quetiapine extended-release tablets are indicated for the treatment of schizophrenia. The efficacy of quetiapine extended-release tablets in schizophrenia was established in one 6-week and one maintenance trial in adults with schizophrenia. Efficacy was supported by three 6-week trials in adults with schizophrenia and one 6-week trial in adolescents with schizophrenia (13 to 17…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4699

What is NDC 70518-4699?
70518-4699 is the product NDC for Quetiapine, Quetiapine fumarate 200 mg/1 tablet, extended release, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Quetiapine.
What is the active ingredient?
Quetiapine fumarate.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Quetiapine?
86 other product NDCs are listed under this name. See all Quetiapine 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 Quetiapine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
QuetiapineQuetiapine fumarate 400 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-470070518-4700-00
QuetiapineQuetiapine fumarate 100 mg/1Tablet, Film coatedOralCoupler LLC67046-048767046-0487-03
QuetiapineQuetiapine fumarate 200 mg/1Tablet, Extended releaseOralCoupler LLC67046-162367046-1623-03
QuetiapineQuetiapine fumarate 300 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-445170518-4451-00
QuetiapineQuetiapine fumarate 400 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-443770518-4437-00
QuetiapineQuetiapine fumarate 50 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-443070518-4430-0070518-4430-01
QuetiapineQuetiapine fumarate 50 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-59868001-0598-06
QuetiapineQuetiapine fumarate 150 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-59968001-0599-06
QuetiapineQuetiapine fumarate 200 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-60068001-0600-06
QuetiapineQuetiapine fumarate 300 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-60168001-0601-06

All 87 Quetiapine NDCs

Other NDCs under ANDA 204253

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

FDA NDC Directory listings under ANDA 204253
ProductStrengthForm · routeLabelerProduct NDC
QuetiapineQuetiapine fumarate 150 mg/1Tablet, Extended releaseOralMacleods Pharmaceuticals Limited33342-134
QuetiapineQuetiapine fumarate 200 mg/1Tablet, Extended releaseOralMacleods Pharmaceuticals Limited33342-135
QuetiapineQuetiapine fumarate 300 mg/1Tablet, Extended releaseOralMacleods Pharmaceuticals Limited33342-136
QuetiapineQuetiapine fumarate 400 mg/1Tablet, Extended releaseOralMacleods Pharmaceuticals Limited33342-137
QuetiapineQuetiapine fumarate 400 mg/1Tablet, Extended releaseOralBryant Ranch Prepack63629-5944
QuetiapineQuetiapine fumarate 400 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-4700
Quetiapine Fumarate ERQuetiapine fumarate 400 mg/1Tablet, Extended releaseOralDirect_Rx72189-642

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