citalopram hydrobromide
Generic: citalopram hydrobromide
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
citalopram hydrobromide
Generic Name
citalopram hydrobromide
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
citalopram hydrobromide 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0238
Product ID
71335-0238_e98dc453-0638-4318-9778-e9a881646d36
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078216
Listing Expiration
2026-12-31
Marketing Start
2007-10-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350238
Hyphenated Format
71335-0238
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
citalopram hydrobromide (source: ndc)
Generic Name
citalopram hydrobromide (source: ndc)
Application Number
ANDA078216 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (71335-0238-1)
- 60 TABLET in 1 BOTTLE (71335-0238-2)
- 90 TABLET in 1 BOTTLE (71335-0238-3)
- 100 TABLET in 1 BOTTLE (71335-0238-4)
- 15 TABLET in 1 BOTTLE (71335-0238-5)
- 120 TABLET in 1 BOTTLE (71335-0238-6)
- 7 TABLET in 1 BOTTLE (71335-0238-7)
Packages (7)
71335-0238-1
30 TABLET in 1 BOTTLE (71335-0238-1)
71335-0238-2
60 TABLET in 1 BOTTLE (71335-0238-2)
71335-0238-3
90 TABLET in 1 BOTTLE (71335-0238-3)
71335-0238-4
100 TABLET in 1 BOTTLE (71335-0238-4)
71335-0238-5
15 TABLET in 1 BOTTLE (71335-0238-5)
71335-0238-6
120 TABLET in 1 BOTTLE (71335-0238-6)
71335-0238-7
7 TABLET in 1 BOTTLE (71335-0238-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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