VECURONIUM BROMIDE
- Product NDC
- 51662-1475
- 11-digit product format
- 516621475
- Labeler code
- 51662
- Product ID
- 51662-1475_9f44bf20-73cc-a2bc-e053-2995a90a27dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VECURONIUM BROMIDE
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA075164
- Marketing category
- ANDA
- Marketing start
- 2019-12-15
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1475-1 | VECURONIUM BROMIDE | 10 mL in 1 VIAL | INJECTION, POWDER, LYOPHILIZED, | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1475 | VECURONIUM BROMIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 2 | Legacy NDC, 1 package rows | 20200224_99c79ed5-94dd-48de-e053-2a95a90a4c64.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 |
|---|
| 51662-1475-1 | 51662147501 | 10 mL in 1 VIAL (51662-1475-1) | 10 ml | 2019-12-15 | 0000-00-00 | No | No | Current |