zolpidem

Generic: zolpidem tartrate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zolpidem
Generic Name zolpidem tartrate
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

zolpidem tartrate 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-691
Product ID 71205-691_f76eb9d8-ca7d-4479-bd16-52a57f623b02
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077214
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2020-09-24

Pharmacologic Class

Classes
central nervous system depression [pe] gaba a agonists [moa] pyridines [cs] gamma-aminobutyric acid-ergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205691
Hyphenated Format 71205-691

Supplemental Identifiers

RxCUI
854873
UPC
0371205691301
UNII
WY6W63843K

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name zolpidem (source: ndc)
Generic Name zolpidem tartrate (source: ndc)
Application Number ANDA077214 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-691-30)
  • 60 TABLET in 1 BOTTLE (71205-691-60)
  • 90 TABLET in 1 BOTTLE (71205-691-90)
source: ndc

Packages (3)

71205-691-30 30 TABLET in 1 BOTTLE (71205-691-30) 71205-691-60 60 TABLET in 1 BOTTLE (71205-691-60) 71205-691-90 90 TABLET in 1 BOTTLE (71205-691-90)

Ingredients (1)

zolpidem tartrate (10 mg/1)

Linked Drug Pages (1)

Zolpidem ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f76eb9d8-ca7d-4479-bd16-52a57f623b02", "openfda": {"upc": ["0371205691301"], "unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["f76eb9d8-ca7d-4479-bd16-52a57f623b02"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-691-30)", "package_ndc": "71205-691-30", "marketing_start_date": "20220830"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-691-60)", "package_ndc": "71205-691-60", "marketing_start_date": "20220830"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-691-90)", "package_ndc": "71205-691-90", "marketing_start_date": "20220830"}], "brand_name": "Zolpidem", "product_id": "71205-691_f76eb9d8-ca7d-4479-bd16-52a57f623b02", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Agonists [MoA]", "Pyridines [CS]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "71205-691", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA077214", "marketing_category": "ANDA", "marketing_start_date": "20200924", "listing_expiration_date": "20261231"}