FOLIC ACID
- Product NDC
- 76413-163
- 11-digit product format
- 764130163
- Labeler code
- 76413
- Product ID
- 76413-163_aca6f39b-8016-40b6-9e16-49fc0a09bd7e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FOLIC ACID
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Central Texas Community Health Centers
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76413-163-30 | FOLIC ACID | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76413-163 | FOLIC ACID TABLET [CENTRAL TEXAS COMMUNITY HEALTH CENTERS] | 2 | Legacy NDC, 1 package rows | 20181010_56ccdc1c-4f85-4b3a-b04b-3f06f37f816a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76413-163-30 | 76413016330 | 30 in 1 BOTTLE | Historical |