Terbutaline Sulfate
- Product NDC
- 17478-933
- 11-digit product format
- 174780933
- Labeler code
- 17478
- Product ID
- 17478-933_42982fe2-3e5c-4ff0-94ad-33e83b7f5b00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Terbutaline Sulfate
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- Akorn
- Application
- ANDA078151
- Marketing category
- ANDA
- Marketing start
- 2010-02-01
- Marketing end
- 0000-00-00
- Substance
- TERBUTALINE SULFATE
- Active strength
- 1 mg/mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-933-01 | 17478093301 | 10 AMPULE in 1 CARTON (17478-933-01) > 1 mL in 1 AMPULE | 10 ampule | 2010-02-01 | 0000-00-00 | No | No | Current |