BENZTROPINE MESYLATE
- Product NDC
- 70518-0649
- 11-digit product format
- 705180649
- Labeler code
- 70518
- Product ID
- 70518-0649_a562f6fb-8a24-2659-e053-2a95a90a514a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZTROPINE MESYLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090168
- Marketing category
- ANDA
- Marketing start
- 2017-07-28
- 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
- 2021-12-31
- 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 |
|---|
| 70518-0649-0 | 70518064900 | 30 TABLET in 1 BLISTER PACK (70518-0649-0) | 30 tablet | 2017-07-28 | 0000-00-00 | No | No | Current |