CYPROHEPTADINE HYDROCHLORIDE
- Product NDC
- 42291-225
- 11-digit product format
- 422910225
- Labeler code
- 42291
- Product ID
- 42291-225_eeb2d277-0622-135f-e053-2995a90a6c1f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYPROHEPTADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA040644
- Marketing category
- ANDA
- Marketing start
- 2010-06-15
- Marketing end
- 2023-02-28
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- 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 |
|---|
| 42291-225-01 | 42291022501 | 100 TABLET in 1 BOTTLE (42291-225-01) | 100 tablet | 2010-06-15 | 0000-00-00 | No | No | Current |
| 42291-225-10 | 42291022510 | 1000 TABLET in 1 BOTTLE (42291-225-10) | 1000 tablet | 2010-06-15 | 0000-00-00 | No | No | Current |