Promethazine Hydrochloride
- Product NDC
- 50090-5362
- 11-digit product format
- 500905362
- Labeler code
- 50090
- Product ID
- 50090-5362_adc38191-6564-4b9e-beea-13c792d566c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- SUPPOSITORY
- Route
- RECTAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040428
- Marketing category
- ANDA
- Marketing start
- 2015-06-01
- 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 |
|---|
| 50090-5362-1 | 50090536201 | 4 BLISTER PACK in 1 CARTON (50090-5362-1) > 1 SUPPOSITORY in 1 BLISTER PACK | 4 blister pack | 2020-11-17 | 0000-00-00 | No | No | Current |
| 50090-5362-2 | 50090536202 | 12 BLISTER PACK in 1 CARTON (50090-5362-2) > 1 SUPPOSITORY in 1 BLISTER PACK | 12 blister pack | 2020-11-17 | 0000-00-00 | No | No | Current |