Akovaz
- Product NDC
- 68001-330
- 11-digit product format
- 680010330
- Labeler code
- 68001
- Product ID
- 68001-330_bca36be2-ff8e-af31-e053-2a95a90a0707
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ephedrine sulfate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- BluePoint Laboratories
- Application
- NDA208289
- Marketing category
- NDA
- Marketing start
- 2017-06-30
- Marketing end
- 2022-11-30
- Substance
- EPHEDRINE SULFATE
- Active strength
- 50 mg/mL
- Pharmacologic classes
- alpha-Adrenergic Agonist [EPC],Adrenergic alpha-Agonists [MoA],beta-Adrenergic Agonist [EPC],Adrenergic beta-Agonists [MoA],Norepinephrine Releasing Agent [EPC],Increased Norepinephrine Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68001-330-60 | 68001033060 | 25 VIAL, SINGLE-DOSE in 1 CARTON (68001-330-60) > 1 mL in 1 VIAL, SINGLE-DOSE (68001-330-59) | 2017-06-30 | 0000-00-00 | No | No | Current |