Benztropine Mesylate
- Product NDC
- 60687-356
- 11-digit product format
- 606870356
- Labeler code
- 60687
- Product ID
- 60687-356_e22204eb-fe59-2032-e053-2995a90a4099
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benztropine mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA204713
- Marketing category
- ANDA
- Marketing start
- 2018-08-31
- 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
- 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 |
|---|
| 60687-356-01 | 60687035601 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-356-01) > 1 TABLET in 1 BLISTER PACK (60687-356-11) | 100 blister pack | 2018-08-31 | 0000-00-00 | No | No | Current |