Hydrocortisone
- Product NDC
- 43749-251
- 11-digit product format
- 437490251
- Labeler code
- 43749
- Product ID
- 43749-251_cb1e7bf4-5d55-5b79-e053-2a95a90a306e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Unipack, Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-09-03
- Marketing end
- 0000-00-00
- Substance
- HYDROCORTISONE
- Active strength
- 0 g/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43749-251 | HYDROCORTISONE MAXIMUM STRENGTH (HYDROCORTISONE) OINTMENT [UNIPACK, INC.] | 1 | Legacy NDC | 20210905_cb1e7bf4-5d54-5b79-e053-2a95a90a306e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43749-251-01 | 43749025101 | 1 TUBE in 1 CARTON (43749-251-01) > 28 g in 1 TUBE (43749-251-03) | 1 tube | 2021-09-03 | 0000-00-00 | No | No | Current |