NDC codes

FDA NDC Directory
Product NDC (as listed)71205-691Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0691Add 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
71205-691-30712050691307120506913030 TABLET in 1 BOTTLE (71205-691-30)Marketed from Aug 30, 2022
71205-691-60712050691607120506916060 TABLET in 1 BOTTLE (71205-691-60)Marketed from Aug 30, 2022
71205-691-90712050691907120506919090 TABLET in 1 BOTTLE (71205-691-90)Marketed from Aug 30, 2022

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)
Zolpidem
Generic name (nonproprietary)
zolpidem tartrate
Active ingredients
Zolpidem tartrate — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 71205
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077214
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Central Nervous System Depression (Physiologic effect)GABA A Agonists (Mechanism)Pyridines (Chemical structure)
Identifiers
Product ID 71205-691_f76eb9d8-ca7d-4479-bd16-52a57f623b02SPL ID f76eb9d8-ca7d-4479-bd16-52a57f623b02SPL set ID f76eb9d8-ca7d-4479-bd16-52a57f623b02RxCUI 854873UNII WY6W63843KUPC 0371205691301
Pharmacologic class
gamma-Aminobutyric Acid-ergic Agonist

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

N471205069130 followed by a unit qualifier and the quantity

Package 71205-0691-30. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Zolpidem Tartrate Tablets is indicated for the short-term treatment of insomnia characterized by difficulties with sleep initiation. Zolpidem Tartrate Tablets has been shown to decrease sleep latency for up to 35 days in controlled clinical studies [see Clinical Studies ( 14 )]. The clinical trials performed in support of efficacy were 4–5 weeks in duration with the final formal assessments of sleep latency performed at the end of treatment. Zolpidem Tartrate Tablets, a gamma-aminobutyric acid (GABA) A receptor positive modulator, is indicated for the short-term treatment of insomnia characterized by difficulties with sleep initiation. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-691

What is NDC 71205-691?
71205-691 is the product NDC for Zolpidem (zolpidem tartrate), Zolpidem tartrate 10 mg/1 tablet, 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?
Zolpidem (Zolpidem Tartrate).
What is the active ingredient?
Zolpidem tartrate.
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 Zolpidem?
15 other product NDCs are listed under this name. See all Zolpidem 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 Zolpidem NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-043080425-0430-0180425-0430-0280425-0430-03
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralBryant Ranch Prepack63629-117063629-1170-01
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralBryant Ranch Prepack63629-899863629-8998-0163629-8998-0263629-8998-03
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralBryant Ranch Prepack63629-899963629-8999-0163629-8999-0263629-8999-03
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralBryant Ranch Prepack63629-961363629-9613-01
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralBryant Ranch Prepack63629-961463629-9614-01
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralACI Healthcare USA, Inc71093-15571093-0155-0471093-0155-06
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralACI Healthcare USA, Inc71093-15671093-0156-0471093-0156-06
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralBryant Ranch Prepack71335-230371335-2303-01
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralBryant Ranch Prepack71335-968471335-9684-0071335-9684-0171335-9684-02+7 more

All 16 Zolpidem NDCs

Other NDCs under ANDA 077214

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

FDA NDC Directory listings under ANDA 077214
ProductStrengthForm · routeLabelerProduct NDC
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralBryant Ranch Prepack63629-1170
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralBryant Ranch Prepack63629-8998
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralBryant Ranch Prepack63629-8999
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralBryant Ranch Prepack63629-9613
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralBryant Ranch Prepack63629-9614
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralACI Healthcare USA, Inc71093-155
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralACI Healthcare USA, Inc71093-156
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralBryant Ranch Prepack71335-2303
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralBryant Ranch Prepack71335-9684
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-670
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-847
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-848
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralBryant Ranch Prepack72162-1982
Zolpidemzolpidem tartrateZolpidem tartrate 10 mg/1TabletOralBryant Ranch Prepack72162-1983
Zolpidemzolpidem tartrateZolpidem tartrate 5 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0430
Zolpidem TartrateZolpidem tartrate 5 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-941
Zolpidem TartrateZolpidem tartrate 10 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-942
Zolpidem TartrateZolpidem tartrate 5 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-904
Zolpidem TartrateZolpidem tartrate 10 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-915
Zolpidem TartrateZolpidem tartrate 5 mg/1Tablet, Film coatedOralThe ACME Laboratories Ltd.72722-103

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