cyproheptadine hydrochloride
- Product NDC
- 23155-703
- 11-digit product format
- 231550703
- Labeler code
- 23155
- Product ID
- 23155-703_d4152712-03ac-45bb-adf9-d2fa1583b90a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyproheptadine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA087056
- Marketing category
- ANDA
- Marketing start
- 2020-01-09
- 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 |
|---|
| 23155-703-01 | 23155070301 | 100 TABLET in 1 BOTTLE (23155-703-01) | 100 tablet | 2020-01-09 | 0000-00-00 | No | No | Current |
| 23155-703-05 | 23155070305 | 500 TABLET in 1 BOTTLE (23155-703-05) | 500 tablet | 2020-01-09 | 0000-00-00 | No | No | Current |
| 23155-703-10 | 23155070310 | 1000 TABLET in 1 BOTTLE (23155-703-10) | 1000 tablet | 2020-01-09 | 0000-00-00 | No | No | Current |