Ciprofloxacin
- Product NDC
- 63739-700
- 11-digit product format
- 637390700
- Labeler code
- 63739
- Product ID
- 63739-700_f201ef0f-6208-33d2-e053-2a95a90a8a95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mckesson Corporation DBA SKY Packaginng
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2007-04-26
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC], Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-700-10 | 63739070010 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-700-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2015-06-10 | 0000-00-00 | No | No | Current |