atomoxetine
Generic: atomoxetine
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
atomoxetine
Generic Name
atomoxetine
Labeler
northstar rx llc
Dosage Form
CAPSULE
Routes
Active Ingredients
atomoxetine hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16714-761
Product ID
16714-761_fc2fb27b-9a53-4df1-874e-bb2ed5157aef
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079019
Listing Expiration
2026-12-31
Marketing Start
2018-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16714761
Hyphenated Format
16714-761
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
atomoxetine (source: ndc)
Generic Name
atomoxetine (source: ndc)
Application Number
ANDA079019 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (16714-761-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc2fb27b-9a53-4df1-874e-bb2ed5157aef", "openfda": {"upc": ["0316714761015", "0316714758015", "0316714759012", "0316714757018", "0316714760018", "0316714755014", "0316714756011"], "unii": ["57WVB6I2W0"], "rxcui": ["349591", "349592", "349593", "349594", "349595", "608139", "608143"], "spl_set_id": ["133a4b65-762b-4712-baba-2442546f0379"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (16714-761-01)", "package_ndc": "16714-761-01", "marketing_start_date": "20180601"}], "brand_name": "atomoxetine", "product_id": "16714-761_fc2fb27b-9a53-4df1-874e-bb2ed5157aef", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "16714-761", "generic_name": "atomoxetine", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA079019", "marketing_category": "ANDA", "marketing_start_date": "20180601", "listing_expiration_date": "20261231"}