Oxymetazoline Hydrochloride
- Product NDC
- 51672-1405
- 11-digit product format
- 516721405
- Labeler code
- 51672
- Product ID
- 51672-1405_40827951-dbc4-4a28-a662-9e08d2cb0dcd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxymetazoline Hydrochloride
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- ANDA213584
- Marketing category
- ANDA
- Marketing start
- 2021-10-04
- Marketing end
- 0000-00-00
- Substance
- OXYMETAZOLINE HYDROCHLORIDE
- Active strength
- 10 mg/g
- Pharmacologic classes
- Vasoconstrictor [EPC],Vasoconstriction [PE],Increased Sympathetic Activity [PE],Imidazolines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 51672-1405 | OXYMETAZOLINE HYDROCHLORIDE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] | 2 | Legacy NDC | 20211012_8a7f2400-5e18-4215-8d2c-f55881706107.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51672-1405-2 | 51672140502 | 1 TUBE in 1 CARTON (51672-1405-2) > 30 g in 1 TUBE | 1 tube | 2021-10-04 | 0000-00-00 | No | No | Current |
| 51672-1405-3 | 51672140503 | 1 TUBE in 1 CARTON (51672-1405-3) > 60 g in 1 TUBE | 1 tube | 2021-10-04 | 0000-00-00 | No | No | Current |