Rocuronium
- Product NDC
- 72162-2263
- 11-digit product format
- 721622263
- Labeler code
- 72162
- Product ID
- 72162-2263_d6b8655a-04b5-46af-a453-0bf3fa8b8b25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rocuronium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210437
- Marketing category
- ANDA
- Marketing start
- 2020-07-20
- Substance
- ROCURONIUM BROMIDE
- Active strength
- 50 mg/5mL
- Pharmacologic classes
- Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Rocuronium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ROCURONIUM BROMIDE | 50 mg/5mL |
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 |
|---|
| 72162-2263-2 | Rocuronium | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 101 |
| 72162-2263-2 | Rocuronium | 5 mL in 1 VIAL | INJECTION, SOLUTION | 5 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2263 | ROCURONIUM INJECTION, SOLUTION [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20240224_6045ed5a-5d2c-4f17-aaba-458fbf87e85c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2263-2 | 72162226302 | 10 VIAL in 1 CARTON (72162-2263-2) / 5 mL in 1 VIAL | 10 vial | 2024-02-23 | No | No | Current |