Vecuronium Bromide
- Product NDC
- 0703-2914
- 11-digit product format
- 007032914
- Labeler code
- 0703
- Product ID
- 0703-2914_ba83a093-2b09-4226-bd09-17f3b7d6a759
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vecuronium Bromide
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Teva Parenteral Medicines, Inc.
- Application
- ANDA074688
- Marketing category
- ANDA
- Marketing start
- 2002-11-14
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0703-2914-03 | 00703291403 | 10 VIAL, SINGLE-USE in 1 CARTON (0703-2914-03) > 10 mL in 1 VIAL, SINGLE-USE (0703-2914-01) | 2002-11-14 | 0000-00-00 | No | No | Current |