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 TABLET, FILM COATED
Routes
ORAL
Active Ingredients

tolterodine tartrate 1 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-805
Product ID 31722-805_c9a8a649-3330-59a0-e053-2995a90ad3c3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204397
Listing Expiration 2026-12-31
Marketing Start 2021-08-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722805
Hyphenated Format 31722-805

Supplemental Identifiers

RxCUI
855178 855194
UPC
0331722806602 0331722805605
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 ANDA204397 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (31722-805-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-805-31)
  • 10 BLISTER PACK in 1 CARTON (31722-805-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-805-32)
  • 500 TABLET, FILM COATED in 1 BOTTLE (31722-805-05)
  • 60 TABLET, FILM COATED in 1 BOTTLE (31722-805-60)
source: ndc

Packages (4)

31722-805-01 10 BLISTER PACK in 1 CARTON (31722-805-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-805-31) 31722-805-02 10 BLISTER PACK in 1 CARTON (31722-805-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-805-32) 31722-805-05 500 TABLET, FILM COATED in 1 BOTTLE (31722-805-05) 31722-805-60 60 TABLET, FILM COATED in 1 BOTTLE (31722-805-60)

Ingredients (1)

tolterodine tartrate (1 mg/1)

Linked Drug Pages (1)

Tolterodine Tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c9a8a649-3330-59a0-e053-2995a90ad3c3", "openfda": {"upc": ["0331722806602", "0331722805605"], "unii": ["5T619TQR3R"], "rxcui": ["855178", "855194"], "spl_set_id": ["f67fce7c-69d3-42ae-8c1d-2e26fd4d7415"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-805-01)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-805-31)", "package_ndc": "31722-805-01", "marketing_start_date": "20210802"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-805-02)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-805-32)", "package_ndc": "31722-805-02", "marketing_start_date": "20210802"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-805-05)", "package_ndc": "31722-805-05", "marketing_start_date": "20210802"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-805-60)", "package_ndc": "31722-805-60", "marketing_start_date": "20210802"}], "brand_name": "Tolterodine Tartrate", "product_id": "31722-805_c9a8a649-3330-59a0-e053-2995a90ad3c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "31722-805", "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": "1 mg/1"}], "application_number": "ANDA204397", "marketing_category": "ANDA", "marketing_start_date": "20210802", "listing_expiration_date": "20261231"}