Benztropine Mesylate
- Product NDC
- 0615-8210
- 11-digit product format
- 006158210
- Labeler code
- 0615
- Product ID
- 0615-8210_d6c7e105-d289-4a17-a650-12b9f333f43e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benztropine mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA204713
- Marketing category
- ANDA
- Marketing start
- 2017-05-15
- 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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8210-39 | 00615821039 | 30 TABLET in 1 BLISTER PACK (0615-8210-39) | 30 tablet | 2018-04-09 | 0000-00-00 | No | No | Current |