Benztropine Mesylate
- Product NDC
- 50090-2792
- 11-digit product format
- 500902792
- Labeler code
- 50090
- Product ID
- 50090-2792_438816b2-1fa9-42c5-a368-e00c3699f471
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benztropine mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040738
- Marketing category
- ANDA
- Marketing start
- 2007-08-27
- Marketing end
- 0000-00-00
- Substance
- BENZTROPINE MESYLATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 50090-2792 | | I | Inactivated by FDA | | 2026-07-31 |
| excluded package | package | 50090-2792 | 50090-2792-0 | D | Discontinued by firm | | 2026-07-31 |
FDA-Initiated Inactive NDC Indexing#