Folic Acid
- Product NDC
- 58118-0137
- 11-digit product format
- 581180137
- Labeler code
- 58118
- Product ID
- 58118-0137_b025952e-f649-48e5-e053-2995a90af83b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FOLIC ACID
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA040796
- Marketing category
- ANDA
- Marketing start
- 2009-01-12
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 58118-0137 | FOLIC ACID TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC] | 7 | Legacy NDC | 20200926_809bdcb3-5b54-4300-9074-2193b66a43f5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-0137-8 | 58118013708 | 30 TABLET in 1 BLISTER PACK (58118-0137-8) | 30 tablet | 2016-09-27 | 0000-00-00 | No | No | Current |