Promethazine Hydrochloride
- Product NDC
- 40085-219
- 11-digit product format
- 400850219
- Labeler code
- 40085
- Product ID
- 40085-219_fc539046-58bc-4530-a688-296333d5c9b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- SUPPOSITORY
- Route
- RECTAL
- Labeler
- Renaissance Pharma, Inc.
- Application
- ANDA040428
- Marketing category
- ANDA
- Marketing start
- 2014-08-01
- Marketing end
- 2020-02-29
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record