ROCURONIUM BROMIDE
- Product NDC
- 51662-1545
- 11-digit product format
- 516621545
- Labeler code
- 51662
- Product ID
- 51662-1545_dc444a4b-16eb-568d-e053-2995a90a53a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ROCURONIUM BROMIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA206206
- Marketing category
- ANDA
- Marketing start
- 2022-04-09
- Substance
- ROCURONIUM BROMIDE
- Active strength
- 100 mg/10mL
- Pharmacologic classes
- Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ROCURONIUM BROMIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ROCURONIUM BROMIDE | 100 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I65MW4OFHZ |
| Rxcui | 1234995 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1545-1 | ROCURONIUM BROMIDE | 10 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1545 | ROCURONIUM BROMIDE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220410_dc444a4b-16ea-568d-e053-2995a90a53a7.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 |
|---|
| 51662-1545-1 | 51662154501 | 10 mL in 1 VIAL, MULTI-DOSE (51662-1545-1) | 10 ml | 2022-04-09 | 0000-00-00 | No | No | Current |