Terbutaline Sulfate
- Product NDC
- 72843-101
- 11-digit product format
- 728430101
- Labeler code
- 72843
- Product ID
- 72843-101_81bce60c-9786-74f5-e053-2a91aa0ade0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Terbutaline Sulfate
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- UBI Pharma Inc.
- Application
- ANDA200122
- Marketing category
- ANDA
- Marketing start
- 2014-12-15
- Marketing end
- 0000-00-00
- Substance
- TERBUTALINE SULFATE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 72843-101-10 | 72843010110 | 10 VIAL in 1 BOX (72843-101-10) > 1 mL in 1 VIAL | 10 vial | 2014-12-15 | 0000-00-00 | No | No | Current |