Terbutaline Sulfate
- Product NDC
- 43063-558
- 11-digit product format
- 430630558
- Labeler code
- 43063
- Product ID
- 43063-558_7d4e8845-0479-42dd-e053-2991aa0aa762
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Terbutaline Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA077152
- Marketing category
- ANDA
- Marketing start
- 2005-03-25
- Marketing end
- 0000-00-00
- Substance
- TERBUTALINE SULFATE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record