bupropion hydrochloride
Generic: bupropion hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
bupropion hydrochloride
Generic Name
bupropion hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
bupropion hydrochloride 150 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2469
Product ID
71335-2469_0c3952f8-d149-4812-bec9-ecf841fe1950
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215568
Listing Expiration
2026-12-31
Marketing Start
2022-12-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352469
Hyphenated Format
71335-2469
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
bupropion hydrochloride (source: ndc)
Generic Name
bupropion hydrochloride (source: ndc)
Application Number
ANDA215568 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 150 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-1)
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-2)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-3)
- 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-4)
- 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-5)
Packages (5)
71335-2469-1
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-1)
71335-2469-2
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-2)
71335-2469-3
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-3)
71335-2469-4
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-4)
71335-2469-5
14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c3952f8-d149-4812-bec9-ecf841fe1950", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["af5b1cc8-f078-4a7b-b64a-4cb2de1e5721"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-1)", "package_ndc": "71335-2469-1", "marketing_start_date": "20241112"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-2)", "package_ndc": "71335-2469-2", "marketing_start_date": "20241112"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-3)", "package_ndc": "71335-2469-3", "marketing_start_date": "20241112"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-4)", "package_ndc": "71335-2469-4", "marketing_start_date": "20241112"}, {"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-5)", "package_ndc": "71335-2469-5", "marketing_start_date": "20241112"}], "brand_name": "Bupropion hydrochloride", "product_id": "71335-2469_0c3952f8-d149-4812-bec9-ecf841fe1950", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "71335-2469", "generic_name": "Bupropion hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA215568", "marketing_category": "ANDA", "marketing_start_date": "20221215", "listing_expiration_date": "20261231"}