Terbutaline Sulfate
- Product NDC
- 52584-665
- 11-digit product format
- 525840665
- Labeler code
- 52584
- Product ID
- 52584-665_0ba29411-e95d-4bee-aee1-e3a135d6aa33
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Terbutaline Sulfate
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA076887
- Marketing category
- ANDA
- Marketing start
- 2011-11-16
- Marketing end
- 2024-03-31
- Substance
- TERBUTALINE SULFATE
- Active strength
- 1 mg/mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-665-01 | 52584066501 | 1 VIAL in 1 BAG (52584-665-01) > 1 mL in 1 VIAL | 1 vial | 2011-11-16 | 2024-03-31 | No | No | Current |