Benztropine Mesylate
- Product NDC
- 63629-2134
- 11-digit product format
- 636292134
- Labeler code
- 63629
- Product ID
- 63629-2134_01ccefa4-8ebc-471d-b9fa-4ba465a7d4a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benztropine mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204713
- Marketing category
- ANDA
- Marketing start
- 2017-05-15
- Marketing end
- 0000-00-00
- Substance
- BENZTROPINE MESYLATE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Anticholinergic [EPC], Antihistamine [EPC], Cholinergic Antagonists [MoA], Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-2134-1 | 63629213401 | 100 TABLET in 1 BOTTLE, PLASTIC (63629-2134-1) | 100 tablet | 2021-03-10 | 0000-00-00 | No | No | Current |