Benztropine
- Product NDC
- 67046-207
- 11-digit product format
- 670460207
- Labeler code
- 67046
- Product ID
- 67046-207_7d65c99d-b04e-77e9-e053-2991aa0a82cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benztropine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA090168
- Marketing category
- ANDA
- Marketing start
- 2017-04-13
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67046-207-30 | Benztropine | 30 in 1 BLISTER PACK | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-207 | BENZTROPINE TABLET [CONTRACT PHARMACY SERVICES-PA] | 2 | Legacy NDC, 1 package rows | 20181221_6a3a8c79-77cb-4f24-e053-2a91aa0a707a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67046-207-30 | 67046020730 | 30 TABLET in 1 BLISTER PACK (67046-207-30) | 30 tablet | 2017-04-13 | 0000-00-00 | No | No | Current |