tolterodine tartrate

Generic: tolterodine tartrate

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

Drug Facts

Product Profile

Brand Name tolterodine tartrate
Generic Name tolterodine tartrate
Labeler camber pharmaceuticals, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

tolterodine tartrate 2 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-607
Product ID 31722-607_e16012ae-5972-470b-8a22-b0626a029e95
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206419
Listing Expiration 2026-12-31
Marketing Start 2017-06-02

Pharmacologic Class

Classes
cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722607
Hyphenated Format 31722-607

Supplemental Identifiers

RxCUI
855182 855189
UPC
0331722607308 0331722607902 0331722607056 0331722608305
UNII
5T619TQR3R

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 tolterodine tartrate (source: ndc)
Generic Name tolterodine tartrate (source: ndc)
Application Number ANDA206419 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-607-05)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-607-30)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-607-90)
source: ndc

Packages (3)

Ingredients (1)

tolterodine tartrate (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e16012ae-5972-470b-8a22-b0626a029e95", "openfda": {"upc": ["0331722607308", "0331722607902", "0331722607056", "0331722608305"], "unii": ["5T619TQR3R"], "rxcui": ["855182", "855189"], "spl_set_id": ["e16012ae-5972-470b-8a22-b0626a029e95"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-607-05)", "package_ndc": "31722-607-05", "marketing_start_date": "20170602"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-607-30)", "package_ndc": "31722-607-30", "marketing_start_date": "20170602"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-607-90)", "package_ndc": "31722-607-90", "marketing_start_date": "20170602"}], "brand_name": "Tolterodine Tartrate", "product_id": "31722-607_e16012ae-5972-470b-8a22-b0626a029e95", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "31722-607", "generic_name": "Tolterodine Tartrate", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolterodine Tartrate", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "2 mg/1"}], "application_number": "ANDA206419", "marketing_category": "ANDA", "marketing_start_date": "20170602", "listing_expiration_date": "20261231"}