Vecuronium Bromide
- Product NDC
- 71288-744
- 11-digit product format
- 712880744
- Labeler code
- 71288
- Product ID
- 71288-744_ef72e810-c31d-4c0a-8a7f-b1cfd8ac15ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vecuronium Bromide
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Meitheal Pharmaceuticals Inc.
- Application
- ANDA074688
- Marketing category
- ANDA
- Marketing start
- 2025-07-01
- Substance
- VECURONIUM BROMIDE
- Active strength
- 10 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
- Vecuronium Bromide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VECURONIUM BROMIDE | 10 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7E4PHP5N1D |
| Rxcui | 859437 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71288-744-10 | Vecuronium Bromide | 10 mL in 1 VIAL, SINGLE-USE | INJECTION, POWDER, LYOPHILIZED, | 10 | | 1 |
| 71288-744-11 | Vecuronium Bromide | 10 in 1 CARTON | INJECTION, POWDER, LYOPHILIZED, | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71288-744-10 | 71288074410 | 10 mL in 1 VIAL, SINGLE-USE | 10 ml | | | | Historical |
| 71288-744-11 | 71288074411 | 10 VIAL, SINGLE-USE in 1 CARTON (71288-744-11) / 10 mL in 1 VIAL, SINGLE-USE (71288-744-10) | | 2025-07-01 | No | No | Current |