Promethazine Hydrochloride
- Product NDC
- 42708-119
- 11-digit product format
- 427080119
- Labeler code
- 42708
- Product ID
- 42708-119_bbb691d7-063f-33bf-e053-2995a90ab5d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA091179
- Marketing category
- ANDA
- Marketing start
- 2011-03-03
- 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
- 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 |
|---|
| 42708-119-12 | 42708011912 | 12 TABLET in 1 BOTTLE (42708-119-12) | 12 tablet | 2018-04-20 | 0000-00-00 | Yes | No | Current |