tolterodine tartrate
Generic: tolterodine tartrate
Labeler: unichem pharmaceuticals (usa), inc.Drug Facts
Product Profile
Brand Name
tolterodine tartrate
Generic Name
tolterodine tartrate
Labeler
unichem pharmaceuticals (usa), inc.
Dosage Form
TABLET
Routes
Active Ingredients
tolterodine tartrate 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
29300-239
Product ID
29300-239_9faf1be0-1f13-47c0-b2aa-3ad62e5037e9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205399
Listing Expiration
2026-12-31
Marketing Start
2020-08-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
29300239
Hyphenated Format
29300-239
Supplemental Identifiers
RxCUI
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
tolterodine tartrate (source: ndc)
Generic Name
tolterodine tartrate (source: ndc)
Application Number
ANDA205399 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 500 TABLET in 1 BOTTLE, PLASTIC (29300-239-05)
- 60 TABLET in 1 BOTTLE, PLASTIC (29300-239-16)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9faf1be0-1f13-47c0-b2aa-3ad62e5037e9", "openfda": {"unii": ["5T619TQR3R"], "rxcui": ["855178", "855194"], "spl_set_id": ["56e62829-5371-416a-90b3-4b6429532d25"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (29300-239-05)", "package_ndc": "29300-239-05", "marketing_start_date": "20200805"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (29300-239-16)", "package_ndc": "29300-239-16", "marketing_start_date": "20200805"}], "brand_name": "Tolterodine Tartrate", "product_id": "29300-239_9faf1be0-1f13-47c0-b2aa-3ad62e5037e9", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "29300-239", "generic_name": "Tolterodine Tartrate", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolterodine Tartrate", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA205399", "marketing_category": "ANDA", "marketing_start_date": "20200805", "listing_expiration_date": "20261231"}