Promethazine Hydrochloride
- Product NDC
- 60760-456
- 11-digit product format
- 607600456
- Labeler code
- 60760
- Product ID
- 60760-456_f06eec16-1c20-815e-e053-2995a90afc14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA040596
- Marketing category
- ANDA
- Marketing start
- 2019-10-09
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-456 | PROMETHAZINE HYDROCHLORIDE TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 2 | Legacy NDC | 20221223_9492e4e9-cda5-64cc-e053-2995a90a04a5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-456-20 | 60760045620 | 20 TABLET in 1 BOTTLE, PLASTIC (60760-456-20) | 20 tablet | 2019-10-09 | 0000-00-00 | No | No | Current |