Promethazine Hydrochloride
- Product NDC
- 68084-154
- 11-digit product format
- 680840154
- Labeler code
- 68084
- Product ID
- 68084-154_e5f7019a-713b-0cf9-e053-2a95a90a8d49
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA040596
- Marketing category
- ANDA
- Marketing start
- 2007-01-10
- Marketing end
- 2023-03-31
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 13 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 |
|---|
| 68084-154-01 | 68084015401 | 100 BLISTER PACK in 1 CARTON (68084-154-01) > 1 TABLET in 1 BLISTER PACK (68084-154-11) | 100 blister pack | 2007-01-10 | 0000-00-00 | No | No | Current |