zolpidem
Generic: zolpidem tartrate
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
zolpidem
Generic Name
zolpidem tartrate
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
zolpidem tartrate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-9684
Product ID
71335-9684_dd311612-26be-4837-ab16-7be1e84fc397
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713359684
Hyphenated Format
71335-9684
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 5 TABLET in 1 BOTTLE (71335-9684-0)
- 30 TABLET in 1 BOTTLE (71335-9684-1)
- 60 TABLET in 1 BOTTLE (71335-9684-2)
- 100 TABLET in 1 BOTTLE (71335-9684-3)
- 50 TABLET in 1 BOTTLE (71335-9684-4)
- 90 TABLET in 1 BOTTLE (71335-9684-5)
- 10 TABLET in 1 BOTTLE (71335-9684-6)
- 15 TABLET in 1 BOTTLE (71335-9684-7)
- 28 TABLET in 1 BOTTLE (71335-9684-8)
- 120 TABLET in 1 BOTTLE (71335-9684-9)
Packages (10)
71335-9684-0
5 TABLET in 1 BOTTLE (71335-9684-0)
71335-9684-1
30 TABLET in 1 BOTTLE (71335-9684-1)
71335-9684-2
60 TABLET in 1 BOTTLE (71335-9684-2)
71335-9684-3
100 TABLET in 1 BOTTLE (71335-9684-3)
71335-9684-4
50 TABLET in 1 BOTTLE (71335-9684-4)
71335-9684-5
90 TABLET in 1 BOTTLE (71335-9684-5)
71335-9684-6
10 TABLET in 1 BOTTLE (71335-9684-6)
71335-9684-7
15 TABLET in 1 BOTTLE (71335-9684-7)
71335-9684-8
28 TABLET in 1 BOTTLE (71335-9684-8)
71335-9684-9
120 TABLET in 1 BOTTLE (71335-9684-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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