PROMETHAZINE HYDROCHLORIDE
- Product NDC
- 60429-151
- 11-digit product format
- 604290151
- Labeler code
- 60429
- Product ID
- 60429-151_eee0307c-1609-2811-e053-2a95a90a1584
- 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
- 2006-07-31
- Marketing end
- 2023-04-30
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 50 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-151-01 | 60429015101 | 100 TABLET in 1 BOTTLE (60429-151-01) | 100 tablet | 2011-11-21 | 0000-00-00 | No | No | Current |