Benztropine Mesylate
- Product NDC
- 70518-1709
- 11-digit product format
- 705181709
- Labeler code
- 70518
- Product ID
- 70518-1709_e5d46dba-3afb-64ff-e053-2a95a90a3441
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benztropine mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204713
- Marketing category
- ANDA
- Marketing start
- 2018-12-04
- 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 |
|---|
| 70518-1709-0 | 70518170900 | 30 TABLET in 1 BLISTER PACK (70518-1709-0) | 30 tablet | 2018-12-04 | 0000-00-00 | No | No | Current |
| 70518-1709-1 | 70518170901 | 100 POUCH in 1 BOX (70518-1709-1) > 1 TABLET in 1 POUCH (70518-1709-2) | 100 pouch | 2021-02-02 | 0000-00-00 | No | No | Current |
| 70518-1709-3 | 70518170903 | 30 TABLET in 1 BLISTER PACK (70518-1709-3) | 30 tablet | 2021-12-09 | 0000-00-00 | No | No | Current |