Folic Acid
- Product NDC
- 58657-150
- 11-digit product format
- 586570150
- Labeler code
- 58657
- Product ID
- 58657-150_9d53033a-114c-79cf-e053-2995a90a2ed1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Method Pharmaceuticals, LLC
- Application
- ANDA091145
- Marketing category
- ANDA
- Marketing start
- 2015-03-01
- 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58657-150-01 | 58657015001 | 100 TABLET in 1 BOTTLE (58657-150-01) | 100 tablet | 2015-03-01 | 0000-00-00 | No | No | Current |
| 58657-150-10 | 58657015010 | 1000 TABLET in 1 BOTTLE (58657-150-10) | 1000 tablet | 2015-03-01 | 0000-00-00 | No | No | Current |