Benztropine Mesylate
- Product NDC
- 70518-1447
- 11-digit product format
- 705181447
- Labeler code
- 70518
- Product ID
- 70518-1447_e909cd8f-f090-1974-e053-2995a90a80e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benztropine mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204713
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- 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 |
|---|
| 70518-1447-1 | 70518144701 | 30 TABLET in 1 BLISTER PACK (70518-1447-1) | 30 tablet | 2019-01-17 | 0000-00-00 | No | No | Current |
| 70518-1447-2 | 70518144702 | 100 POUCH in 1 BOX (70518-1447-2) > 1 TABLET in 1 POUCH (70518-1447-3) | 100 pouch | 2021-02-02 | 0000-00-00 | No | No | Current |
| 70518-1447-4 | 70518144704 | 28 TABLET in 1 BLISTER PACK (70518-1447-4) | 28 tablet | 2021-02-25 | 0000-00-00 | No | No | Current |