CYPROHEPTADINE HYDROCHLORIDE
- Product NDC
- 55700-700
- 11-digit product format
- 557000700
- Labeler code
- 55700
- Product ID
- 55700-700_24f85056-bea6-43ac-805d-a37dc76e5898
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYPROHEPTADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA208938
- Marketing category
- ANDA
- Marketing start
- 2017-07-20
- Marketing end
- 0000-00-00
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-700-60 | 55700070060 | 60 TABLET in 1 BOTTLE (55700-700-60) | 60 tablet | 2018-11-09 | 0000-00-00 | No | No | Current |