Promethazine Hydrochloride
- Product NDC
- 0121-0927
- 11-digit product format
- 001210927
- Labeler code
- 0121
- Product ID
- 0121-0927_e20b6b57-77e4-1370-e053-2a95a90ae5e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- ANDA040643
- Marketing category
- ANDA
- Marketing start
- 2020-09-18
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 6 mg/5mL
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0121-0927-16 | 00121092716 | 473 mL in 1 BOTTLE (0121-0927-16) | 473 ml | 2020-10-09 | 0000-00-00 | No | No | Current |