PROMETHAZINE HYDROCHLORIDE
- Product NDC
- 50090-4124
- 11-digit product format
- 500904124
- Labeler code
- 50090
- Product ID
- 50090-4124_173f3614-86f0-4db8-b94f-7887ea70ee70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- promethazine hydrochloride
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA087953
- Marketing category
- ANDA
- Marketing start
- 1982-11-15
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 6 mg/5mL
- 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 |
|---|
| 50090-4124-0 | 50090412400 | 473 mL in 1 BOTTLE, PLASTIC (50090-4124-0) | 473 ml | 2019-02-04 | 0000-00-00 | No | No | Current |