atomoxetine

Generic: atomoxetine

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atomoxetine
Generic Name atomoxetine
Labeler camber pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

atomoxetine hydrochloride 40 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-717
Product ID 31722-717_bdf74b27-8e7e-e4d6-e053-2a95a90a7b1a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202682
Listing Expiration 2026-12-31
Marketing Start 2021-03-11

Pharmacologic Class

Classes
norepinephrine reuptake inhibitor [epc] norepinephrine uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722717
Hyphenated Format 31722-717

Supplemental Identifiers

RxCUI
349591 349592 349593 349594 349595 608139 608143
UPC
0331722714303 0331722715300 0331722716307 0331722718301 0331722720304 0331722719308 0331722717304
UNII
57WVB6I2W0

Packaging Origin

Original Packager
true

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 ANDA202682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (31722-717-30)
source: ndc

Packages (1)

31722-717-30 30 CAPSULE in 1 BOTTLE (31722-717-30)

Ingredients (1)

atomoxetine hydrochloride (40 mg/1)

Linked Drug Pages (1)

Atomoxetine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bdf74b27-8e7e-e4d6-e053-2a95a90a7b1a", "openfda": {"upc": ["0331722714303", "0331722715300", "0331722716307", "0331722718301", "0331722720304", "0331722719308", "0331722717304"], "unii": ["57WVB6I2W0"], "rxcui": ["349591", "349592", "349593", "349594", "349595", "608139", "608143"], "spl_set_id": ["f266ab7b-5a68-42b5-b204-e3249bea0aed"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (31722-717-30)", "package_ndc": "31722-717-30", "marketing_start_date": "20210311"}], "brand_name": "Atomoxetine", "product_id": "31722-717_bdf74b27-8e7e-e4d6-e053-2a95a90a7b1a", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "31722-717", "generic_name": "Atomoxetine", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA202682", "marketing_category": "ANDA", "marketing_start_date": "20210311", "listing_expiration_date": "20261231"}