Ranitidine
- Product NDC
- 60505-0160
- 11-digit product format
- 605050160
- Labeler code
- 60505
- Product ID
- 60505-0160_026bd1d9-8f27-d47a-a738-9298aab03e0d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA075167
- Marketing category
- ANDA
- Marketing start
- 2016-12-22
- Marketing end
- 2022-07-12
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 60505-0160-3 | 60505016003 | 1 BLISTER PACK in 1 CARTON (60505-0160-3) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2016-12-22 | 2022-07-12 | No | No | Current |
| 60505-0160-4 | 60505016004 | 3 BLISTER PACK in 1 CARTON (60505-0160-4) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 3 blister pack | 2016-12-22 | 2022-07-12 | No | No | Current |