THALLOUS CHLORIDE TL 201
- Product NDC
- 17156-299
- 11-digit product format
- 171560299
- Labeler code
- 17156
- Product ID
- 17156-299_d1490ed9-5cf7-454f-acd1-a2716140dba2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Thallous Chloride Tl-201
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medi-Physics, Inc. dba GE Healthcare
- Application
- NDA018110
- Marketing category
- NDA
- Marketing start
- 1982-02-01
- Marketing end
- 0000-00-00
- Substance
- THALLOUS CHLORIDE TL-201
- Active strength
- 1 mCi/mL
- Pharmacologic classes
- Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA]
- 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 |
|---|
| 17156-299-16 | 17156029916 | 6.6 mL in 1 VIAL (17156-299-16) | 6.6 ml | 1982-02-01 | 0000-00-00 | No | No | Current |
| 17156-299-18 | 17156029918 | 8.8 mL in 1 VIAL (17156-299-18) | 8.8 ml | 1982-02-01 | 0000-00-00 | No | No | Current |