Cyproheptadine Hydrochloride
- Product NDC
- 66689-333
- 11-digit product format
- 666890333
- Labeler code
- 66689
- Product ID
- 66689-333_13701068-9041-4e3e-a2f9-e650140bea7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- VistaPharm, LLC
- Application
- ANDA209108
- Marketing category
- ANDA
- Marketing start
- 2019-07-29
- Marketing end
- 0000-00-00
- Substance
- CYPROHEPTADINE
- Active strength
- 2 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 66689-333-16 | 66689033316 | 473 mL in 1 BOTTLE (66689-333-16) | 473 ml | 2019-07-29 | 0000-00-00 | No | No | Current |