Promethazine Hydrochloride
- Product NDC
- 63629-8187
- 11-digit product format
- 636298187
- Labeler code
- 63629
- Product ID
- 63629-8187_91f3038d-b817-4cd7-bdad-9aac93fc150c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040596
- Marketing category
- ANDA
- Marketing start
- 2005-12-14
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-8187-1 | 63629818701 | 12 TABLET in 1 BOTTLE (63629-8187-1) | 12 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |