Promethazine Hydrochloride
- Product NDC
- 63629-6875
- 11-digit product format
- 636296875
- Labeler code
- 63629
- Product ID
- 63629-6875_8cbdada0-ef23-4a10-8630-4f1ffcf8fa85
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091179
- Marketing category
- ANDA
- Marketing start
- 2011-03-03
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-6875-1 | 63629687501 | 30 TABLET in 1 BOTTLE (63629-6875-1) | 30 tablet | 2015-12-30 | 0000-00-00 | No | No | Current |
| 63629-6875-2 | 63629687502 | 20 TABLET in 1 BOTTLE (63629-6875-2) | 20 tablet | 2015-12-30 | 0000-00-00 | No | No | Current |