Ranitidine
- Product NDC
- 60505-2881
- 11-digit product format
- 605052881
- Labeler code
- 60505
- Product ID
- 60505-2881_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
- 2005-01-24
- 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 |
|---|
| 60505-2881-3 | 60505288103 | 1 BOTTLE in 1 CARTON (60505-2881-3) > 30 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2005-01-24 | 2022-07-12 | No | No | Current |
| 60505-2881-7 | 60505288107 | 1 BOTTLE in 1 CARTON (60505-2881-7) > 1000 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2005-01-24 | 2022-07-12 | No | No | Current |
| 60505-2881-8 | 60505288108 | 1 BOTTLE in 1 CARTON (60505-2881-8) > 80 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2005-01-24 | 2022-07-12 | No | No | Current |