Rocuronium Bromide
- Product NDC
- 70756-669
- 11-digit product format
- 707560669
- Labeler code
- 70756
- Product ID
- 70756-669_45959358-88cf-4717-9683-87b6aa987bf9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rocuronium Bromide
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Lifestar Pharma LLC
- Application
- ANDA219674
- Marketing category
- ANDA
- Marketing start
- 2025-05-29
- 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
- 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 | 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 |
|---|
| 70756-669-10 | Rocuronium Bromide | 10 in 1 CARTON | INJECTION | 10 | | 4 |
| 70756-669-10 | Rocuronium Bromide | 5 mL in 1 VIAL | INJECTION | 5 | | 4 |
| 70756-669-85 | Rocuronium Bromide | 1 in 1 CARTON | INJECTION | 1 | | 4 |
| 70756-669-85 | Rocuronium Bromide | 5 mL in 1 VIAL | INJECTION | 5 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70756-669-10 | 70756066910 | 10 VIAL in 1 CARTON (70756-669-10) / 5 mL in 1 VIAL | 10 vial | 2025-05-29 | No | No | Current |
| 70756-669-85 | 70756066985 | 1 VIAL in 1 CARTON (70756-669-85) / 5 mL in 1 VIAL | 1 vial | 2025-05-29 | No | No | Current |