Promethazine
- Product NDC
- 43063-708
- 11-digit product format
- 430630708
- Labeler code
- 43063
- Product ID
- 43063-708_d2ba3e81-6401-23eb-e053-2995a90afdaa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- SUPPOSITORY
- Route
- RECTAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040428
- Marketing category
- ANDA
- Marketing start
- 2015-02-17
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-708-02 | 43063070802 | 2 SUPPOSITORY in 1 BOTTLE, PLASTIC (43063-708-02) | 2 suppository | 2016-09-22 | 0000-00-00 | No | No | Current |