Trospium Chloride
- Product NDC
- 0904-7059
- 11-digit product format
- 009047059
- Labeler code
- 0904
- Product ID
- 0904-7059_239e206f-f6ca-4b35-a5b0-46d255cd57fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trospium Chloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA204945
- Marketing category
- ANDA
- Marketing start
- 2015-11-16
- Substance
- TROSPIUM CHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Trospium Chloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TROSPIUM CHLORIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1E6682427E |
| Rxcui | 857560 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-7059-52 | Trospium Chloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7059 | TROSPIUM CHLORIDE TABLET, FILM COATED [MAJOR PHARMACEUTICALS] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250216_35ae4d64-4625-4fdd-a2d4-e20b87c56876.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7059-52 | 00904705952 | 60 TABLET, FILM COATED in 1 BOTTLE (0904-7059-52) | 2015-11-16 | 0000-00-00 | No | No | Current |