NA
- Product NDC
- 83090-007
- 11-digit product format
- 830900007
- Labeler code
- 83090
- Product ID
- 83090-007_eff2e41b-a181-2c76-e053-2995a90aa8b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- RETROBULBAR
- Labeler
- Sintetica US LLC
- Application
- ANDA214269
- Marketing category
- ANDA
- Marketing start
- 2022-11-15
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 83090-007-01 | NA | 5 mL in 1 AMPULE | INJECTION, SOLUTION | 5 | | 1 |
| 83090-007-10 | NA | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83090-007 | NA (LIDOCAINE HYDROCHLORIDE) INJECTION, SOLUTION [SINTETICA US LLC] | 1 | Legacy NDC, 2 package rows | 20221217_a7529e5b-47b1-4148-98dd-65aecc33a8c3.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 |
|---|
| 83090-007-01 | 83090000701 | 5 mL in 1 AMPULE | 5 ml | | | | | Historical |
| 83090-007-10 | 83090000710 | 10 AMPULE in 1 CARTON (83090-007-10) > 5 mL in 1 AMPULE (83090-007-01) | 10 ampule | 2022-11-15 | 0000-00-00 | No | No | Current |