MOXIFLOXACIN HYDROCHLORIDE
NDC 71335-2329, moxifloxacin hydrochloride, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-2329
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202632
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2329 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MOXIFLOXACIN HYDROCHLORIDE400 mg/1
Pharmacologic classes
Fluoroquinolone Antibacterial [EPC]; Fluoroquinolones [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-2329-1 | 71335232901 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-2329-1) |
| 71335-2329-2 | 71335232902 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2329-2) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6cd420c3-113e-4fc2-b59f-bfc7c485c14d
Use it
Look up 71335-2329 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2329 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2329. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.