What is NDC 16729-148?

16729-148 is the product NDC for Quetiapine, Quetiapine fumarate 200 mg/1 tablet, film coated, listed with the FDA by Accord Healthcare Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Accord Healthcare Inc., NDC labeler code 16729. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Quetiapine NDC 16729-148 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)16729-148Labeler and product segments. Claims need a package NDC.

Product NDC at billing width16729-0148Add 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
16729-148-01	1672901480116729014801	100 TABLET, FILM COATED in 1 BOTTLE (16729-148-01)Marketed from Jul 21, 2015
16729-148-17	1672901481716729014817	1000 TABLET, FILM COATED in 1 BOTTLE (16729-148-17)Marketed from Mar 28, 2012

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): Quetiapine
Generic name (nonproprietary): quetiapine
Active ingredients: Quetiapine fumarate — 200 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Accord Healthcare Inc.NDC labeler code 16729
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202152
Marketing start: Mar 28, 2012
Listing expires: Dec 31, 2026
Identifiers: Product ID 16729-148_438f950d-730b-8926-e063-6294a90a8f66SPL ID 438f950d-730b-8926-e063-6294a90a8f66SPL set ID 2d77412a-e084-4406-ac33-d882aece9354RxCUI 312743, 312744, 312745, 317174, 616483, 616487UNII 2S3PL1B6UJUPC 0316729150101, 0316729147101, 0316729146104, 0316729145107, 0316729148108
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

N416729014801 followed by a unit qualifier and the quantity

Package 16729-0148-01. 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 Nov 14, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Quetiapine tablet is an atypical antipsychotic indicated for the treatment of: Schizophrenia ( 1.1 ) Bipolar I disorder manic episodes ( 1.2 ) Bipolar disorder, depressive episodes ( 1.2 ) 1.1 Schizophrenia Quetiapine tablet is indicated for the treatment of schizophrenia. The efficacy of quetiapine tablets in schizophrenia was established in three 6-week trials in adults and one 6-week trial in adolescents (13 to 17 years). The effectiveness of quetiapine tablets for the maintenance treatment of schizophrenia has not been systematically evaluated in controlled clinical trials [see Clinical Studies (14.1) ]. 1.2 Bipolar Disorder Quetiapine tablet is indicated for the acute treatment of manic…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 16729-148

What is NDC 16729-148?: 16729-148 is the product NDC for Quetiapine, Quetiapine fumarate 200 mg/1 tablet, film coated, listed with the FDA by Accord Healthcare Inc.. It has 2 package NDCs, 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?: Accord Healthcare Inc., NDC labeler code 16729. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Quetiapine	Quetiapine fumarate 400 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4700	70518-4700-00
Quetiapine	Quetiapine fumarate 200 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4699	70518-4699-00
Quetiapine	Quetiapine fumarate 100 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0487	67046-0487-03
Quetiapine	Quetiapine fumarate 200 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1623	67046-1623-03
Quetiapine	Quetiapine fumarate 300 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4451	70518-4451-00
Quetiapine	Quetiapine fumarate 400 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4437	70518-4437-00
Quetiapine	Quetiapine fumarate 50 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4430	70518-4430-0070518-4430-01
Quetiapine	Quetiapine fumarate 50 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-598	68001-0598-06
Quetiapine	Quetiapine fumarate 150 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-599	68001-0599-06
Quetiapine	Quetiapine fumarate 200 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-600	68001-0600-06

All 87 Quetiapine NDCs

Other NDCs under ANDA 202152

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

FDA NDC Directory listings under ANDA 202152
Product	Strength	Form · route	Labeler	Product NDC
Quetiapine fumarate	Quetiapine fumarate 25 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-452
Quetiapine	Quetiapine fumarate 400 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-7116
Quetiapine fumarate	Quetiapine fumarate 50 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-219
Quetiapine fumarate	Quetiapine fumarate 100 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-269
Quetiapine Fumarate	Quetiapine fumarate 100 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-4776
Quetiapine Fumarate	Quetiapine fumarate 50 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-4841
Quetiapine Fumarate	Quetiapine fumarate 200 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-4964
Quetiapine	Quetiapine fumarate 25 mg/1	Tablet, Film coatedOral	Accord Healthcare Inc.	16729-145
Quetiapine	Quetiapine fumarate 50 mg/1	Tablet, Film coatedOral	Accord Healthcare Inc.	16729-146
Quetiapine	Quetiapine fumarate 100 mg/1	Tablet, Film coatedOral	Accord Healthcare Inc.	16729-147
Quetiapine	Quetiapine fumarate 300 mg/1	Tablet, Film coatedOral	Accord Healthcare Inc.	16729-149
Quetiapine	Quetiapine fumarate 400 mg/1	Tablet, Film coatedOral	Accord Healthcare Inc.	16729-150
Quetiapine	Quetiapine fumarate 200 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-401