Benztropine Mesylate
- Product NDC
- 70518-1455
- 11-digit product format
- 705181455
- Labeler code
- 70518
- Product ID
- 70518-1455_92df42fe-d670-9a34-e053-2995a90ac868
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benztropine mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040715
- Marketing category
- ANDA
- Marketing start
- 2018-10-02
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1455 | BENZTROPINE MESYLATE TABLET [REMEDYREPACK INC.] | 6 | Legacy NDC | 20250223_e26f5e65-d577-43cd-8ab8-da298a4b0a58.zip |