PROMETHAZINE HYDROCHLORIDE
- Product NDC
- 60429-149
- 11-digit product format
- 604290149
- Labeler code
- 60429
- Product ID
- 60429-149_c59bb097-5358-1944-e053-2995a90a4193
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- promethazine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA040712
- Marketing category
- ANDA
- Marketing start
- 2007-05-04
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 13 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 |
|---|
| 60429-149-01 | 60429014901 | 100 TABLET in 1 BOTTLE (60429-149-01) | 100 tablet | 2011-11-21 | 0000-00-00 | No | No | Current |