Folic Acid
- Product NDC
- 50268-345
- 11-digit product format
- 502680345
- Labeler code
- 50268
- Product ID
- 50268-345_ddcc34d0-3324-2c56-e053-2995a90ac47d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA040625
- Marketing category
- ANDA
- Marketing start
- 2010-04-28
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-345-15 | 50268034515 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-345-15) > 1 TABLET in 1 BLISTER PACK (50268-345-11) | 50 blister pack | 2018-04-28 | 0000-00-00 | No | No | Current |