Cyproheptadine Hydrochloride
- Product NDC
- 71335-0211
- 11-digit product format
- 713350211
- Labeler code
- 71335
- Product ID
- 71335-0211_331121b2-93ff-410f-9f42-aa4814e5ffb6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206553
- Marketing category
- ANDA
- Marketing start
- 2017-01-17
- Marketing end
- 0000-00-00
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71335-0211-1 | 71335021101 | 30 TABLET in 1 BOTTLE (71335-0211-1) | 30 tablet | 2017-06-28 | 0000-00-00 | No | No | Current |
| 71335-0211-2 | 71335021102 | 60 TABLET in 1 BOTTLE (71335-0211-2) | 60 tablet | 2017-06-28 | 0000-00-00 | No | No | Current |
| 71335-0211-3 | 71335021103 | 28 TABLET in 1 BOTTLE (71335-0211-3) | 28 tablet | 2017-06-28 | 0000-00-00 | No | No | Current |
| 71335-0211-4 | 71335021104 | 100 TABLET in 1 BOTTLE (71335-0211-4) | 100 tablet | 2017-06-28 | 0000-00-00 | No | No | Current |
| 71335-0211-5 | 71335021105 | 90 TABLET in 1 BOTTLE (71335-0211-5) | 90 tablet | 2017-06-28 | 0000-00-00 | No | No | Current |