Benazepril Hydrochloride
- Product NDC
- 55700-317
- 11-digit product format
- 557000317
- Labeler code
- 55700
- Product ID
- 55700-317_6a2416b5-2e7c-4a3f-a837-57b7e7070bca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA076118
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55700-317-30 | Benazepril Hydrochloride | 30 in 1 BOTTLE | TABLET, COATED | 30 | | 1 |
| 55700-317-90 | Benazepril Hydrochloride | 90 in 1 BOTTLE | TABLET, COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-317 | BENAZEPRIL HYDROCHLORIDE TABLET, COATED [LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC] | 1 | Legacy NDC, 1 package rows | 20161122_e5747e8f-b1b9-4caf-9f43-36dd8401adc6.zip |
| 55700-317 | BENAZEPRIL HYDROCHLORIDE TABLET, COATED [LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC] | 1 | Legacy NDC, 1 package rows | 20160223_722df1e3-b160-4920-9469-a6070bb5e538.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55700-317-30 | 55700031730 | 30 in 1 BOTTLE | Historical |
| 55700-317-90 | 55700031790 | 90 in 1 BOTTLE | Historical |