vecuronium bromide
- Product NDC
- 47335-932
- 11-digit product format
- 473350932
- Labeler code
- 47335
- Product ID
- 47335-932_82d6bc45-04a5-409a-9223-da1884b2468f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vecuronium bromide
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA079001
- Marketing category
- ANDA
- Marketing start
- 2014-12-15
- Substance
- VECURONIUM BROMIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 47335-932-40 | vecuronium bromide | 20 mL in 1 VIAL | INJECTION, POWDER, LYOPHILIZED, | 20 | | 5 |
| 47335-932-44 | vecuronium bromide | 10 in 1 BOX | INJECTION, POWDER, LYOPHILIZED, | 10 | | 5 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| VECURONIUM BROMIDE | ACTIVE INGREDIENT | 7E4PHP5N1D | VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SUN PHARMA GLOBAL FZE] | 1 | |
| VECURONIUM | ACTIVE MOIETY | 5438723848 | VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SUN PHARMA GLOBAL FZE] | 1 | |
| ANHYDROUS CITRIC ACID | INACTIVE INGREDIENT | XF417D3PSL | VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SUN PHARMA GLOBAL FZE] | 1 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SUN PHARMA GLOBAL FZE] | 1 | |
| PHOSPHORIC ACID | INACTIVE INGREDIENT | E4GA8884NN | VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SUN PHARMA GLOBAL FZE] | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SUN PHARMA GLOBAL FZE] | 1 | |
| SODIUM PHOSPHATE, DIBASIC, ANHYDROUS | INACTIVE INGREDIENT | 22ADO53M6F | VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SUN PHARMA GLOBAL FZE] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47335-932 | VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SUN PHARMACEUTICAL INDUSTRIES, INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20181025_a14da3ee-a731-4282-be9d-407473517470.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 |
|---|
| 47335-932-40 | 47335093240 | 20 mL in 1 VIAL | 20 ml | | | | | Historical |
| 47335-932-44 | 47335093244 | 10 VIAL in 1 BOX (47335-932-44) / 20 mL in 1 VIAL (47335-932-40) | 10 vial | 2014-12-15 | 0000-00-00 | No | No | Current |