DOPAMINE HYDROCHLORIDE
- Product NDC
- 51662-1490
- 11-digit product format
- 516621490
- Labeler code
- 51662
- Product ID
- 51662-1490_11c32f50-2496-3a8e-e063-6394a90a9a78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOPAMINE HYDROCHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA207707
- Marketing category
- ANDA
- Marketing start
- 2021-07-10
- Substance
- DOPAMINE HYDROCHLORIDE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Catecholamine [EPC], Catecholamines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DOPAMINE HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOPAMINE HYDROCHLORIDE | 40 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7L3E358N9L |
| Rxcui | 1743938 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1490-1 | DOPAMINE HYDROCHLORIDE | 10 mL in 1 VIAL, SINGLE-DOSE | INJECTION | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1490 | DOPAMINE HYDROCHLORIDE INJECTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240220_c6c8539b-0da9-2d97-e053-2a95a90a3aa8.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 |
|---|
| 51662-1490-1 | 51662149001 | 10 mL in 1 VIAL, SINGLE-DOSE (51662-1490-1) | 10 ml | 2021-07-10 | 0000-00-00 | No | No | Current |