CYPROHEPTADINE HYDROCHLORIDE
- Product NDC
- 71335-1859
- 11-digit product format
- 713351859
- Labeler code
- 71335
- Product ID
- 71335-1859_dddfd253-84c8-453f-bdf0-410315ab9145
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYPROHEPTADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040644
- Marketing category
- ANDA
- Marketing start
- 2013-10-21
- Marketing end
- 2024-01-31
- 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 |
|---|
| 71335-1859-1 | 71335185901 | 30 TABLET in 1 BOTTLE (71335-1859-1) | 30 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |
| 71335-1859-2 | 71335185902 | 60 TABLET in 1 BOTTLE (71335-1859-2) | 60 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |
| 71335-1859-3 | 71335185903 | 28 TABLET in 1 BOTTLE (71335-1859-3) | 28 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |
| 71335-1859-4 | 71335185904 | 100 TABLET in 1 BOTTLE (71335-1859-4) | 100 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |
| 71335-1859-5 | 71335185905 | 90 TABLET in 1 BOTTLE (71335-1859-5) | 90 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |