Cyproheptadine Hydrochloride
- Product NDC
- 0527-1949
- 11-digit product format
- 005271949
- Labeler code
- 0527
- Product ID
- 0527-1949_06a06ff1-54cb-427a-b208-7e3cce78d398
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA203191
- Marketing category
- ANDA
- Marketing start
- 2017-07-13
- Marketing end
- 2024-01-31
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 2 mg/5mL
- 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 |
|---|
| 0527-1949-47 | 00527194947 | 473 mL in 1 BOTTLE, PLASTIC (0527-1949-47) | 473 ml | 2017-07-13 | 2024-01-31 | No | No | Current |