TOFRANIL
- Product NDC
- 0406-9922
- 11-digit product format
- 004069922
- Labeler code
- 0406
- Product ID
- 0406-9922_cd0e9158-8287-4d4a-870b-9518cdd140f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- imipramine hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- SpecGx LLC
- Application
- ANDA087846
- Marketing category
- ANDA
- Marketing start
- 1984-05-22
- Marketing end
- 2021-12-31
- Substance
- IMIPRAMINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0406-9922-01 | 00406992201 | 100 TABLET, SUGAR COATED in 1 BOTTLE (0406-9922-01) | 1984-05-22 | 0000-00-00 | No | No | Current |
| 0406-9922-03 | 00406992203 | 30 TABLET, SUGAR COATED in 1 BOTTLE (0406-9922-03) | 1984-05-22 | 0000-00-00 | No | No | Current |