Phospholine Iodide
- Product NDC
- 0046-1065
- 11-digit product format
- 000461065
- Labeler code
- 0046
- Product ID
- 0046-1065_d6430e45-82f7-41b6-8db8-4d6f486303f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- echothiophate iodide
- Dosage form
- KIT
- Labeler
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Application
- NDA011963
- Marketing category
- NDA
- Marketing start
- 1959-12-04
- Marketing end
- 2022-06-30
- Active strength
- 0
- 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 |
|---|
| 0046-1065-05 | 00046106505 | 1 KIT in 1 KIT (0046-1065-05) * 6.25 mL in 1 BOTTLE (0046-1465-05) * 5 mL in 1 BOTTLE (0046-1162-05) | 1 kit | 1959-12-04 | 0000-00-00 | No | No | Current |