Benztropine Mesylate
- Product NDC
- 70518-1691
- 11-digit product format
- 705181691
- Labeler code
- 70518
- Product ID
- 70518-1691_e5d1dbce-aaca-a811-e053-2995a90adb4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benztropine mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204713
- Marketing category
- ANDA
- Marketing start
- 2018-11-26
- 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 |
|---|
| 70518-1691-1 | 70518169101 | 28 TABLET in 1 BLISTER PACK (70518-1691-1) | 28 tablet | 2019-01-25 | 0000-00-00 | No | No | Current |
| 70518-1691-2 | 70518169102 | 60 TABLET in 1 BLISTER PACK (70518-1691-2) | 60 tablet | 2020-11-03 | 0000-00-00 | No | No | Current |
| 70518-1691-3 | 70518169103 | 100 POUCH in 1 BOX (70518-1691-3) > 1 TABLET in 1 POUCH (70518-1691-4) | 100 pouch | 2022-03-17 | 0000-00-00 | No | No | Current |