What is NDC 71205-384?

71205-384 is the product NDC for Eszopiclone, Eszopiclone 1 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Eszopiclone?

89 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Eszopiclone NDC 71205-384 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-384Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0384Add 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
71205-384-30	71205038430	30 TABLET, FILM COATED in 1 BOTTLE (71205-384-30)Marketed from Jan 10, 2020
71205-384-60	71205038460	60 TABLET, FILM COATED in 1 BOTTLE (71205-384-60)Marketed from Jan 10, 2020
71205-384-90	71205038490	90 TABLET, FILM COATED in 1 BOTTLE (71205-384-90)Marketed from Jan 10, 2020

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): Eszopiclone
Generic name (nonproprietary): eszopiclone
Active ingredients: Eszopiclone — 1 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208451
Marketing start: Sep 15, 2016
Listing expires: Dec 31, 2026
DEA schedule: CIV
Identifiers: Product ID 71205-384_7fe5e114-9285-4448-a98e-24820b998749SPL ID 7fe5e114-9285-4448-a98e-24820b998749SPL set ID 024f833e-c20c-46a2-971b-3f2a716b1678RxCUI 485440UNII UZX80K71OEUPC 0371205384609

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

N471205038430 followed by a unit qualifier and the quantity

Package 71205-0384-30. 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 Jun 1, 2022. This label includes a boxed warning.

Indications (excerpt from the label)

Eszopiclone tablets are indicated for the treatment of insomnia. In controlled outpatient and sleep laboratory studies, eszopiclone tablets administered at bedtime decreased sleep latency and improved sleep maintenance. The clinical trials performed in support of efficacy were up to 6 months in duration. The final formal assessments of sleep latency and maintenance were performed at 4 weeks in the 6-week study (adults only), at the end of both 2-week studies (elderly only) and at the end of the 6-month study (adults only). Eszopiclone tablets are indicated for the treatment of insomnia. Eszopiclone tablets has been shown to decrease sleep latency and improve sleep maintenance (1)…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-384

What is NDC 71205-384?: 71205-384 is the product NDC for Eszopiclone, Eszopiclone 1 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Eszopiclone.
What is the active ingredient?: Eszopiclone.
Who is the labeler?: Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Eszopiclone?: 89 other product NDCs are listed under this name. See all Eszopiclone 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 Eszopiclone NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Eszopiclone	Eszopiclone 2 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4398	70518-4398-00
Eszopiclone	Eszopiclone 2 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4361	70518-4361-0070518-4361-01
Eszopiclone	Eszopiclone 1 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8826	68788-8826-0368788-8826-06
Eszopiclone	Eszopiclone 1 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0407	80425-0407-0180425-0407-0280425-0407-03
Eszopiclone	Eszopiclone 1 mg/1	Tablet, Film coatedOral	Proficient Rx LP	82804-159	82804-0159-3082804-0159-6082804-0159-90
Eszopiclone	Eszopiclone 1 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-855	31722-0855-0131722-0855-30
Eszopiclone	Eszopiclone 2 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-856	31722-0856-0131722-0856-30
Eszopiclone	Eszopiclone 3 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-857	31722-0857-0131722-0857-30
Eszopiclone	Eszopiclone 1 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8387	68788-8387-0368788-8387-06
Eszopiclone	Eszopiclone 3 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-3576	70518-3576-0070518-3576-0170518-3576-02

All 90 Eszopiclone NDCs

Other NDCs under ANDA 208451

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

FDA NDC Directory listings under ANDA 208451
Product	Strength	Form · route	Labeler	Product NDC
Eszopiclone	Eszopiclone 2 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-513
Eszopiclone	Eszopiclone 1 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-967
Eszopiclone	Eszopiclone 2 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-968
Eszopiclone	Eszopiclone 3 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-969
Eszopiclone	Eszopiclone 3 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-236
Eszopiclone	Eszopiclone 2 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0063
Eszopiclone	Eszopiclone 3 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0066
Eszopiclone	Eszopiclone 3 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-067
Eszopiclone	Eszopiclone 2 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-1310
Eszopiclone	Eszopiclone 3 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-3514
Eszopiclone	Eszopiclone 1 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7744
Eszopiclone	Eszopiclone 2 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7745
Eszopiclone	Eszopiclone 3 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7746
Eszopiclone	Eszopiclone 1 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-9659
Eszopiclone	Eszopiclone 1 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals, Inc.	68788-7667