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FOLIC ACID

NDC 71205-913, FOLIC ACID, tablet, from Proficient Rx LP.

Product NDC
71205-913
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040796
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-913 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FOLIC ACID1 mg/1
Package NDCNDC-11Package
71205-913-0071205091300100 TABLET in 1 BOTTLE (71205-913-00)
71205-913-11712050913111000 TABLET in 1 BOTTLE (71205-913-11)
71205-913-307120509133030 TABLET in 1 BOTTLE (71205-913-30)
71205-913-5571205091355500 TABLET in 1 BOTTLE (71205-913-55)
71205-913-607120509136060 TABLET in 1 BOTTLE (71205-913-60)
71205-913-907120509139090 TABLET in 1 BOTTLE (71205-913-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/607d23e8-21ef-4d73-88f1-990cf267d22e

Use it

Look up 71205-913 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-913 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-913. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.