BENZTROPINE MESYLATE
- Product NDC
- 70518-0720
- 11-digit product format
- 705180720
- Labeler code
- 70518
- Product ID
- 70518-0720_e21e015d-2e11-cb77-e053-2995a90ad237
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZTROPINE MESYLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090168
- Marketing category
- ANDA
- Marketing start
- 2017-08-31
- 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 |
|---|
| 70518-0720-0 | 70518072000 | 30 TABLET in 1 BLISTER PACK (70518-0720-0) | 30 tablet | 2017-08-31 | 0000-00-00 | No | No | Current |
| 70518-0720-1 | 70518072001 | 28 TABLET in 1 BLISTER PACK (70518-0720-1) | 28 tablet | 2018-09-17 | 0000-00-00 | No | No | Current |
| 70518-0720-2 | 70518072002 | 60 TABLET in 1 BLISTER PACK (70518-0720-2) | 60 tablet | 2018-10-16 | 0000-00-00 | No | No | Current |